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FDA 510(k)

IMC CABLE/WIRE COVER

K-Number: K933382 · 1994-01-27

ApplicantInman Medical Corp.
Decision Date1994-01-27
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

IMC CABLE/WIRE COVER 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 1994-01-27 under 510(k) number K933382. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMC CABLE/WIRE COVER?

IMC CABLE/WIRE COVER is a medical device that received FDA 510(k) clearance on 1994-01-27. The listed applicant is Inman Medical Corp.. The 510(k) number is K933382.

When did IMC CABLE/WIRE COVER receive FDA 510(k) clearance?

IMC CABLE/WIRE COVER received FDA 510(k) clearance on 1994-01-27, under 510(k) number K933382.

Who is the listed applicant for IMC CABLE/WIRE COVER?

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 CABLE/WIRE COVER?

The FDA product code for IMC CABLE/WIRE COVER is KKX.

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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/FILTERK933774IMC SALINE WET DRESSINGK933305IMC 5.0MM IRRIGATION/ASPIRATION PROBEK933306IMC 5.0MM IRRIGATION/ASPIRATION PROBE W/HOLES

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Related Devices (Code: KKX)

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.

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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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