510(k) · Cleared

Recalled · Class I · 2009

Pediatric Instatrak System

K981998510(k) TraditionalCleared Aug 21, 199874-day reviewClass II21 CFR 892.2050Recalls 1 (1 Class I)

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Visualization Technology, Inc. · LLZ System, Image Processing, Radiological

Cleared on Aug 21, 1998 as substantially equivalent to K960330 (Visualization Technology, Inc., 1996) and 1 other predicate after a 74-day review. Its family tree reaches back 1 generation to 1994. 9 of the 330 devices in its family, counting itself, have a Class I recall. 327 later devices descend from it. It has been recalled once, including a Class I recall.

Decided: Aug 21, 1998
Review: 74 days
Class: Class II
Product code: LLZ
Recalls: 1 (1 Class I)
Predicates: 2

Its longest line of descent runs back 1 generation to K911783 (1994). 2 ancestors in all. 327 later devices descend from it, 4 citing it directly. 9 of the 330 devices in this family, counting this one, have a Class I recall.

By dateBy generation

Root · 1 generation backK911783 Allegro Viewing WandI.S.G. Technologies, Inc. · 1994
This deviceK981998 Pediatric Instatrak SystemVisualization Technology, Inc. · 1998
Descendant · cites it directly · 325 of its ownK983529 Instatrak 3000Visualization Technology, Inc. · 1998 · Recalled (Class I)
Descendant · 2 generations on · 294 of its ownK994270 Instatrak 3000 System with Fluorotrak Module, Model IT3000Visualization Technology, Inc. · 2000 · Recalled (Class I)
Descendant · cites it directly · 280 of its ownK982994 Skull Base Instatrak SystemVisualization Technology, Inc. · 1998 · Recalled (Class I)
Descendant · cites it directly · 278 of its ownK053610 AbarisTraxtal Technologies, Inc. · 2006 · Recalled
Descendant · 2 generations on · 222 of its ownK121498 PercunavPhilips Health Care · 2012

Showing 5 of 327 descendants. See all descendants

Descendants cleared per year

1998high 35 (2020) · low 0 (2001)2026

Class I recalls in this family

K960330 Instatrakdirect predicate · 1996
K983529 Instatrak 3000cites it directly · 1998
K990919 Straight Aspirator, 90 Degree Aspirator,45…cites it directly · 1999
K982994 Skull Base Instatrak Systemcites it directly · 1998

Most influential descendants

Showing 5 of 327 · See all

K983529Instatrak 3000Visualization Technology, Inc. · 1998 · cites it directly325descendants
K994270Instatrak 3000 System with Fluorotrak Module, Model IT3000Visualization Technology, Inc. · 2000 · 2 generations on294descendants
K982994Skull Base Instatrak SystemVisualization Technology, Inc. · 1998 · cites it directly280descendants
K053610AbarisTraxtal Technologies, Inc. · 2006 · cites it directly278descendants
K121498PercunavPhilips Health Care · 2012 · 2 generations on222descendants

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
−1	K911783	Allegro Viewing Wand	I.S.G. Technologies, Inc.	1994	—
0 (this device)	K981998	Pediatric Instatrak System	Visualization Technology, Inc.	1998	—
+1	K983529	Instatrak 3000	Visualization Technology, Inc.	1998	Class I
+2	K994270	Instatrak 3000 System with Fluorotrak Module, Model IT3000	Visualization Technology, Inc.	2000	Class I
+1	K982994	Skull Base Instatrak System	Visualization Technology, Inc.	1998	Class I
+1	K053610	Abaris	Traxtal Technologies, Inc.	2006	3
+2	K121498	Percunav	Philips Health Care	2012	—

Other ancestors by year cleared

Year cleared	Devices	With a Class I recall
1996	1	1

Descendants by year cleared

Year cleared	Devices	With a Class I recall
1998	2	2
1999	1	1
2000	1	1
2002	1	1
2004	1	0
2006	3	0
2008	2	0
2009	2	0
2010	2	0
2011	2	0
2012	6	0
2013	4	0
2014	12	0
2015	18	0
2016	23	0
2017	34	0
2018	22	0
2019	17	0
2020	35	0
2021	26	0
2022	24	0
2023	19	0
2024	19	0
2025	28	2
2026	23	0

FIG. 1 — Lineage of K981998, 1994–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

9 devices in this family have a Class I recall. A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new LLZ device

#1 K230955 syngo Application Softwarescore 21.5 · 11 generations · no Class I recall
#2 Held for the reportin the report
#3 Held for the reportin the report

Get a 510(k) Report

What was it cleared against? (2)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

Type	Number	Device	Applicant	Decided	Recalls
*	K960330	Instatrak Summary page 1 …uted Tomography X-Ray System 3. IDENTIFICATION OF THE PREDICATE OR LEGALLY MARKETED DEVICE(S) TO WHICH EQUIVALENCE IS BEING CLAIMED Adult InstaTrak System, subject of K960330 and the Viewing Wand manufactured by ISG Technologies, Inc., subject of K911783. Visualization Technology, Inc. 510(k) 6/5/98 Pe…	Visualization Technology, Inc.	1996	Class I
*	K911783	Allegro Viewing Wand Summary page 1 …ETED DEVICE(S) TO WHICH EQUIVALENCE IS BEING CLAIMED Adult InstaTrak System, subject of K960330 and the Viewing Wand manufactured by ISG Technologies, Inc., subject of K911783. Visualization Technology, Inc. 510(k) 6/5/98 Pediatric InstaTrak System Page D-1 4, DEVICE DESCRIPTION The Ins…	I.S.G. Technologies, Inc.	1994	—

Also cleared against K960330: 7 other devices →

What descends from it? (327)

See all 327

4 later devices cite it directly; ranked here by how many devices descend from each in turn.

Number	Device	Applicant	Decided	Descendants
K983529	Instatrak 3000 Class I	Visualization Technology, Inc.	1998	325
K982994	Skull Base Instatrak System Class I	Visualization Technology, Inc.	1998	280
K053610	Abaris	Traxtal Technologies, Inc.	2006	278
K990919	Straight Aspirator, 90 Degree Aspirator,45 Degree Aspirator,7 French Aspirator,Extended… Class I	Visualization Technology, Inc.	1999	0

Has anything in its family been recalled? (9 Class I)

Recalls of this device

Date	Class	Recall	Root cause	Reason
Jun 22, 2009	Class I	Z-2251-2012	Labeling False and Misleading	GE Healthcare Surgery had discovered that using the Inverted Headset Placement is not a validated configuration with the IT 3000, 2500, 2500 plus, 3500, 3500 plus, ConneCTstat, and ConneCTstat Plus Surgical Navigation equipment.

Relatives with a Class I recall

Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.

K960330InstatrakVisualization Technology, Inc. · 1996 · Direct predicate · ◆ in the 1996 ancestors bar of FIG. 11 Class I recall
K983529Instatrak 3000Visualization Technology, Inc. · 1998 · Cites it directly · ◆ in the 1998 descendants bar of FIG. 11 Class I recall
K990919Straight Aspirator, 90 Degree Aspirator,45 Degree Aspirator,7 French Aspirator,Extended Straight…Visualization Technology, Inc. · 1999 · Cites it directly · ◆ in the 1999 descendants bar of FIG. 11 Class I recall
K982994Skull Base Instatrak SystemVisualization Technology, Inc. · 1998 · Cites it directly · ◆ in the 1998 descendants bar of FIG. 11 Class I recall
K994270Instatrak 3000 System with Fluorotrak Module, Model IT3000Visualization Technology, Inc. · 2000 · 2 generations on · ◆ in the 2000 descendants bar of FIG. 12 Class I recalls
K022069Oec Fluorotrak 9800 PlusGe Oec Medical Systems · 2002 · 3 generations on · ◆ in the 2002 descendants bar of FIG. 11 Class I recall
K242670Lumify Diagnostic Ultrasound SystemPhilips Ultrasound · 2025 · 8 generations on · ◆ in the 2025 descendants bar of FIG. 11 Class I recall
K242519Lumify Diagnostic Ultrasound SystemPhilips Ultrasound · 2025 · 8 generations on · ◆ in the 2025 descendants bar of FIG. 11 Class I recall

Nearest 5 of 8; all are on the web page.

What does this lineage say?

1 of the 2 ancestors has a recall of any class; 1 has a Class I recall.
Of its descendants, K983529 (Visualization Technology, Inc., 1998) has gone furthest, with 325 descendants of its own.
7 other devices also cite its predicate K960330.

How does its category compare?

All LLZ devices

LLZ System, Image Processing, Radiological: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · LLZ

58in 2025

2007high 106 (2011) · low 51 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LLZ

173in 2025

2007high 173 (2025) · low 36 (2007)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · LLZ

11in 2025

2007high 64 (2013) · low 2 (2019)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · LLZ

116in 2025

2007high 15,631 (2014) · low 26 (2023)2025

MAUDE reports naming product code LLZ, not matched to any one device; reports are not rates.

View these four charts as a table

Year	Decisions	Median 510(k) review, days	Recalls (Class I)	MAUDE reports
2007	76	36	20	152
2008	94	52	32	154
2009	70	62	21	145
2010	51	98	17	145
2011	106	79	30	454
2012	82	87	12	266
2013	95	84	64	1,130
2014	78	89	6	15,631
2015	64	90	16	211
2016	82	90	12	290
2017	78	107	5	104
2018	104	105	7	72
2019	74	107	2	88
2020	81	115	6	82
2021	83	116	3	70
2022	65	137	4	28
2023	87	157	8	26
2024	62	131	6	42
2025	58	173	11	116
2026	45	110	14	—

What is it indicated for?

The Pediatric InstaTrak System is intended for image guided assistance cluring nasal surgery in pediatric patients. It is intended to be used during the treatment of acute and chronic sinusitis, endoscopic dacryocystorhinostomy, optic nerve and orbital decompression, the removal of polyps, the biopsy and removal of tumors, and the repair of CSF leaks, pituitary disorder and encephalocele.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

https://510kreport.com/device/K981998 · printed Nov 6, 2026

Cite this page

510(k) Report. “K981998: Pediatric Instatrak System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K981998

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Record history

FDA decision record loaded May 2, 2026
Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
Lineage and recalls computed Nov 3, 2026
Page last updated Nov 3, 2026