IMC 5.0MM IRRIGATION/ASPIRATION PROBE— 510(k) K933305

Name: FDA 510(k) clearance K933305
Creator: U.S. Food and Drug Administration
Published: 1993-10-05

Substantially Equivalent

Inman Medical Corp.

FDA 510(k) clearance K933305 for IMC 5.0MM IRRIGATION/ASPIRATION PROBE, Substantially Equivalent on 1993-10-05. Applicant: Inman Medical Corp.. Device class: 1.

Clearance details

Applicant: Inman Medical Corp.
Product code: Code GCY
Device class: Class 1
Regulation: 21 CFR 878.4680
Advisory panel: General, Plastic Surgery
Date received: 1993-07-07
Decision date: 1993-10-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fort Worth, TX, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GCY

view all

K972703 — REDYROB-CLOSED WOUND DRAINAGE SYSTEM1997-10-01
K971036 — ODONTIT AUTOGENOUS BONE COLLECTION DEVICE1997-06-03
K963839 — CORDIS SUCTION RESERVOIR - MODEL NUMBER: 910-5001996-12-12
K960099 — PENROSE DRAIN MODELS 6001 - 60071996-03-11
K950754 — MACRO SUCTION TUBE MODEL NO 100611995-04-25

More clearances from Inman Medical Corp.

view all

K933171 — INMAN IRRIGATION TAPERED PROBE1994-04-29
K933169 — INMAN ENDOSCOPIC BLUNT DISSECTOR1994-04-19
K933094 — INSUFFLATOR TUBING KIT W/FILTER1994-04-18
K933382 — IMC CABLE/WIRE COVER1994-01-27
K933774 — IMC SALINE WET DRESSING1993-11-08

Adverse events under product code GCY

product code GCY

Malfunction: 786
Other: 1
Total: 787

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.