510(k) Report

510(k) · Cleared

Cleared

10.0MM Suction/Irrigation Probe & Tubing Kit

K932762510(k) TraditionalCleared Aug 31, 199384-day reviewClass II21 CFR 876.1500

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

Inman Medical Corp. · GCS Endoscope, Battery-Powered And Accessories

Cleared on Aug 31, 1993 after an 84-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

Decided
Aug 31, 1993
Review
84 days
Class
Class II
Product code
GCS
Recalls
None
Predicates
0

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

FIG. 1 — Lineage of K932762Source: FDA 510(k) database · How lineage is built

Get the monthly Device Review Tracker

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 GCS? 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
Get a 510(k) Report

What was it cleared against?

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

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.

How does its category compare?

All GCS devices

GCS Endoscope, Battery-Powered And Accessories: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · GCS

FDA has decided no GCS device since 2007.

Median 510(k) review, days · GCS

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

Recalls per year · GCS

No recall names GCS since 2007.

Adverse event reports per year · GCS

No MAUDE report names GCS since 2007.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20170—00
20180—00
20190—00
20200—00
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—

More from Inman Medical Corp.

14 FDA decisions under this applicant name. See the company

  • K933171Inman Irrigation Tapered ProbeInman Medical Corp. · 1994
  • K933169Inman Endoscopic Blunt DissectorInman Medical Corp. · 1994
  • K933094Insufflator Tubing Kit W/FilterInman Medical Corp. · 1994
  • K933382Imc Cable/Wire CoverInman Medical Corp. · 1994
  • K933774Imc Saline Wet DressingInman Medical Corp. · 1993

Recent decisions in GCS

The GCS category page

  • K944062Laprascopic GrasperInstrument Makar, Inc. · 1995
  • K944067Peanut Wand, ModificationIdeal Medical, Inc. · 1994
  • K933201Aesculap Trocar Instrument SetAesculap, Inc. · 1993
  • K933371Imc Endoscopic Instrument HolderInman Medical Corp. · 1993
  • K924134Leisegang Laparoscopic Irrigation System/AccessLeisegang Medical, Inc. · 1993

https://510kreport.com/device/K932762 · printed Nov 5, 2026

Cite this page

510(k) Report. “K932762: 10.0MM Suction/Irrigation Probe & Tubing Kit.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K932762

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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