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FDA 510(k)

END-O-FOG ENDOSCOPIC FOG ELIMINATION SYSTEM

K-Number: K943927 · 1994-09-16

ApplicantAmerican Hydro-Surgical Instruments, Inc.
Decision Date1994-09-16
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

END-O-FOG ENDOSCOPIC FOG ELIMINATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is American Hydro-Surgical Instruments, Inc.. It received FDA 510(k) clearance on 1994-09-16 under 510(k) number K943927. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the END-O-FOG ENDOSCOPIC FOG ELIMINATION SYSTEM?

END-O-FOG ENDOSCOPIC FOG ELIMINATION SYSTEM is a medical device that received FDA 510(k) clearance on 1994-09-16. The listed applicant is American Hydro-Surgical Instruments, Inc.. The 510(k) number is K943927.

When did END-O-FOG ENDOSCOPIC FOG ELIMINATION SYSTEM receive FDA 510(k) clearance?

END-O-FOG ENDOSCOPIC FOG ELIMINATION SYSTEM received FDA 510(k) clearance on 1994-09-16, under 510(k) number K943927.

Who is the listed applicant for END-O-FOG ENDOSCOPIC FOG ELIMINATION SYSTEM?

The FDA 510(k) record lists American Hydro-Surgical Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for END-O-FOG ENDOSCOPIC FOG ELIMINATION SYSTEM?

The FDA product code for END-O-FOG ENDOSCOPIC FOG ELIMINATION SYSTEM is GCJ.

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Official Source

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

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