510(k) Report

510(k) · Cleared

Cleared

Exact-Touch

K915844510(k) TraditionalCleared Jan 7, 1994743-day reviewClass II21 CFR 884.4530

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

Baal Assoc., Inc. · HHT Spatula, Cervical, Cytological

Cleared on Jan 7, 1994 after a 743-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.

Decided
Jan 7, 1994
Review
743 days
Class
Class II
Product code
HHT
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 1998: 1 descendant cleared1990200020102020
  1. This deviceK915844 Exact-TouchBaal Assoc., Inc. · 1994
  2. Descendant · cites it directly · 0 of its ownK983181 CytoprepCytoprep Inc. Est. · 1998

Most influential descendants

Showing 1 of 1 · See all
  • K983181CytoprepCytoprep Inc. Est. · 1998 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K915844Exact-TouchBaal Assoc., Inc.1994—
+1K983181CytoprepCytoprep Inc. Est.1998—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199810
FIG. 1 — Lineage of K915844, 1994–1998Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

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

Planning a device in HHT? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

  • Candidate predicates for a device like this, rankedin the report
  • Recall history across each candidate’s familyin the report
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What was it cleared against?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K983181CytoprepCytoprep Inc. Est.19980

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • Of its descendants, K983181 (Cytoprep Inc. Est., 1998) has gone furthest, with 0 descendants of its own.

How does its category compare?

All HHT devices

HHT Spatula, Cervical, Cytological: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · HHT

1in 2019

2007: 12008: 22009: 12012: 12015: 12017: 12019: 1
2007high 2 (2008) · low 0 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HHT

Too few HHT 510(k)s in any year since 2007 to give a median.

Recalls per year · HHT

No recall names HHT since 2007.

Adverse event reports per year · HHT

1in 2025

2007: 22008: 32009: 12010: 12011: 12014: 12016: 62017: 12018: 12019: 32020: 32023: 52024: 12025: 1
2007high 6 (2016) · low 0 (2012)2025

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

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20071—02
20082—03
20091—01
20100—01
20110—01
20121—00
20130—00
20140—01
20151—00
20160—06
20171—01
20180—01
20191—03
20200—03
20210—00
20220—00
20230—05
20240—01
20250—01
20260—0—
Cite this page

510(k) Report. “K915844: Exact-Touch.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K915844

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026