510(k) · Cleared

Cleared

Scintillation Gamma Camera

K140206510(k) TraditionalCleared May 8, 2014101-day reviewClass II21 CFR 892.1200

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

Ddd-Diagnostic A/S · KPS System, Tomography, Computed, Emission

Cleared on May 8, 2014 as substantially equivalent to K001888 (Danish Diagnostic Development A/S, 2000) after a 101-day review. Its family tree reaches back 1 generation to 2000. 1 later device descends from it.

Decided: May 8, 2014
Review: 101 days
Class: Class II
Product code: KPS
Recalls: None
Predicates: 1

Its longest line of descent runs back 1 generation to K001888 (2000). 1 later device descends from it, 1 citing it directly.

By dateBy generation

Root · 1 generation backK001888 Unicorn Model SYS0630Danish Diagnostic Development A/S · 2000
This deviceK140206 Scintillation Gamma CameraDdd-Diagnostic A/S · 2014
Descendant · cites it directly · 0 of its ownK161674 QuantumCamDdd-Diagnostic A/S · 2016

Most influential descendants

Showing 1 of 1 · See all

K161674QuantumCamDdd-Diagnostic A/S · 2016 · cites it directly0descendants

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
−1	K001888	Unicorn Model SYS0630	Danish Diagnostic Development A/S	2000	—
0 (this device)	K140206	Scintillation Gamma Camera	Ddd-Diagnostic A/S	2014	—
+1	K161674	QuantumCam	Ddd-Diagnostic A/S	2016	—

Descendants by year cleared

Year cleared	Devices	With a Class I recall
2016	1	0

FIG. 1 — Lineage of K140206, 2000–2016Source: 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.

Planning a device in KPS? 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 KPS device

#1 K253564 uMI Panvivo (uMI Panvivo); uMI Panvivo (uMI…score 18.6 · 17 generations · no Class I recall
#2 Held for the reportin the report
#3 Held for the reportin the report

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What was it cleared against? (1)

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
*	K001888	Unicorn Model SYS0630 Summary page 1 …3 Predicate Device: UNICORN MODEL SYS0630 (later renamed as meridian), DDD-Diagnostic A/s 510(k) Number: K001888 4 Device description: The QuantumCam is a general purpose dual detector gamma camera…	Danish Diagnostic Development A/S	2000	—

Also cleared against K001888: 1 other device →

What descends from it? (1)

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

Number	Device	Applicant	Decided	Descendants
K161674	QuantumCam	Ddd-Diagnostic A/S	2016	0

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?

Its one ancestor has no recall.
Of its descendants, K161674 (Ddd-Diagnostic A/S, 2016) has gone furthest, with 0 descendants of its own.
1 other device also cites its predicate K001888.

How does its category compare?

All KPS devices

KPS System, Tomography, Computed, Emission: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, this device’s year, is highlighted.

FDA decisions per year · KPS

12in 2025

2007high 17 (2008) · low 3 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KPS

65in 2025

2007high 112 (2015) · low 25 (2008)2026

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

Recalls per year · KPS

16in 2025

2007high 34 (2011) · low 4 (2010)2026

Class I (17 since 2007) Class II/III not classified

Adverse event reports per year · KPS

36in 2025

2007high 240 (2013) · low 10 (2016)2025

MAUDE reports naming product code KPS, 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	8	38	22	38
2008	17	25	16	11
2009	9	42	14	15
2010	3	91	4	44
2011	7	28	34	56
2012	6	94	13	34
2013	11	84	13	240
2014	11	92	18	33
2015	3	112	5	24
2016	11	65	16	10
2017	11	104	11	31
2018	13	59	12 (3)	26
2019	3	60	5 (5)	105
2020	12	72	8	22
2021	15	66	4	10
2022	5	60	8 (6)	15
2023	12	63	6 (3)	22
2024	11	59	15	23
2025	12	65	16	36
2026	6	67	6	—

What is it indicated for?

The QuantumCam is a gamma camera system designed to acquire data for whole body static, gated

or dynamic and multi-slice images. The system is intended for use as diagnostic imaging device.

When used with appropriate radio pharmaceuticals, images are produced representing the internal

distribution of radioactivity in head or body. The system allows you to acquire data for high resolution

three dimensional, static, gated or dynamic images of biochemical and metabolic processes using Tc-

99m, TI-201, 1-123, In-ill1, Ga-67, Co-57.

Indications for use as stated in the FDA summary.

https://510kreport.com/device/K140206 · printed Nov 6, 2026

Cite this page

510(k) Report. “K140206: Scintillation Gamma Camera.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K140206

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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