510(k) Report

510(k) · Cleared

Cleared

Panoret, Model PNM 60

K040325510(k) SpecialCleared Mar 8, 200427-day reviewClass II21 CFR 886.1120

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

Medibell Medical Vision Technologies, Ltd. · HKI Camera, Ophthalmic, Ac-Powered

Cleared on Mar 8, 2004 as substantially equivalent to K001111 (Cmt Medical Technologies, Ltd., 2000) after a 27-day review. Its family tree reaches back 1 generation to 2000.

Decided
Mar 8, 2004
Review
27 days
Class
Class II
Product code
HKI
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K001111 (2000). No later device cites it as a predicate yet.

K001111 · Panoret, Model 1000A · Cmt Medical Technologies, Ltd. · 20002000200220042006
  1. Root · 1 generation backK001111 Panoret, Model 1000ACmt Medical Technologies, Ltd. · 2000
  2. This deviceK040325 Panoret, Model PNM 60Medibell Medical Vision Technologies, Ltd. · 2004
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K001111Panoret, Model 1000ACmt Medical Technologies, Ltd.2000—
0 (this device)K040325Panoret, Model PNM 60Medibell Medical Vision Technologies, Ltd.2004—
FIG. 1 — Lineage of K040325, 2000–2004Source: 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), 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 HKI? 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 HKI device

  1. #1 K253176 TearViewscore 12.7 · 5 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #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.

TypeNumberDeviceApplicantDecidedRecalls
*K001111Panoret, Model 1000ACmt Medical Technologies, Ltd.2000—

What descends from it?

No later submission names this one as a predicate yet.

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.

How does its category compare?

All HKI devices

HKI Camera, Ophthalmic, Ac-Powered: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · HKI

4in 2025

2007: 22008: 52009: 112010: 62011: 72012: 52013: 72014: 42016: 42017: 22018: 62019: 42020: 52021: 42022: 12023: 52024: 32025: 42026 (partial year): 2
2007high 11 (2009) · low 0 (2015)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HKI

167in 2025

2008: 29 days median2009: 104 days median2010: 140 days median2011: 160 days median2012: 179 days median2013: 141 days median2014: 135 days median2016: 146 days median2018: 71 days median2019: 73 days median2020: 182 days median2021: 155 days median2023: 259 days median2024: 28 days median2025: 167 days median
2007high 259 (2023) · low 28 (2024)2026

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

Recalls per year · HKI

1in 2018

2012: 12016: 12017: 12018: 1
2007high 1 (2012) · low 0 (2007)2026

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

Adverse event reports per year · HKI

1in 2023

2007: 32008: 12009: 12012: 22013: 222014: 32015: 32016: 662017: 202018: 142020: 52021: 32022: 12023: 1
2007high 66 (2016) · low 0 (2010)2025

MAUDE reports naming product code HKI, 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
20072—03
200852901
20091110401
2010614000
2011716000
2012517912
20137141022
2014413503
20150—03
20164146166
20172—120
2018671114
201947300
2020518205
2021415503
20221—01
2023525901
202432800
2025416700
20262—0—

What is it indicated for?

The PNM 60 is a diagnostic device indicated to provide digital photographs of the interior of the eye as well as the anterior segment and external part of the eye.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K040325: Panoret, Model PNM 60.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K040325

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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