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FDA 510(k)

IMC 5.0MM IRRIGATION/ASPIRATION PROBE

K-Number: K933305 · 1993-10-05

ApplicantInman Medical Corp.
Decision Date1993-10-05
Product CodeGCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

IMC 5.0MM IRRIGATION/ASPIRATION PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Inman Medical Corp.. It received FDA 510(k) clearance on 1993-10-05 under 510(k) number K933305. The device is classified under product code GCY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMC 5.0MM IRRIGATION/ASPIRATION PROBE?

IMC 5.0MM IRRIGATION/ASPIRATION PROBE is a medical device that received FDA 510(k) clearance on 1993-10-05. The listed applicant is Inman Medical Corp.. The 510(k) number is K933305.

When did IMC 5.0MM IRRIGATION/ASPIRATION PROBE receive FDA 510(k) clearance?

IMC 5.0MM IRRIGATION/ASPIRATION PROBE received FDA 510(k) clearance on 1993-10-05, under 510(k) number K933305.

Who is the listed applicant for IMC 5.0MM IRRIGATION/ASPIRATION PROBE?

The FDA 510(k) record lists Inman Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IMC 5.0MM IRRIGATION/ASPIRATION PROBE?

The FDA product code for IMC 5.0MM IRRIGATION/ASPIRATION PROBE is GCY.

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Other records listing Inman Medical Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K933171INMAN IRRIGATION TAPERED PROBEK933169INMAN ENDOSCOPIC BLUNT DISSECTORK933094INSUFFLATOR TUBING KIT W/FILTERK933382IMC CABLE/WIRE COVERK933774IMC SALINE WET DRESSINGK933306IMC 5.0MM IRRIGATION/ASPIRATION PROBE W/HOLES

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Related Devices (Code: GCY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K972703REDYROB-CLOSED WOUND DRAINAGE SYSTEMB.Braun Medical, Inc.K971036ODONTIT AUTOGENOUS BONE COLLECTION DEVICEInterpore Intl.K963839CORDIS SUCTION RESERVOIR - MODEL NUMBER: 910-500Cordis Corp.K960099PENROSE DRAIN MODELS 6001 - 6007Sil-Med Corp.K950754MACRO SUCTION TUBE MODEL NO 10061Dlp, Inc.K936223PRESSURE IRRIGATING SYSTEMLevel 1 Technologies, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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