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FDA 510(k)

ENDOSCOPIC ANTI-FOG KIT, 100-302-00

K-Number: K933520 · 1993-08-24

ApplicantAvail-Southwest Division
Decision Date1993-08-24
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENDOSCOPIC ANTI-FOG KIT, 100-302-00 is the device name listed in this FDA 510(k) record. The listed applicant is Avail-Southwest Division. It received FDA 510(k) clearance on 1993-08-24 under 510(k) number K933520. 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 ENDOSCOPIC ANTI-FOG KIT, 100-302-00?

ENDOSCOPIC ANTI-FOG KIT, 100-302-00 is a medical device that received FDA 510(k) clearance on 1993-08-24. The listed applicant is Avail-Southwest Division. The 510(k) number is K933520.

When did ENDOSCOPIC ANTI-FOG KIT, 100-302-00 receive FDA 510(k) clearance?

ENDOSCOPIC ANTI-FOG KIT, 100-302-00 received FDA 510(k) clearance on 1993-08-24, under 510(k) number K933520.

Who is the listed applicant for ENDOSCOPIC ANTI-FOG KIT, 100-302-00?

The FDA 510(k) record lists Avail-Southwest Division as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENDOSCOPIC ANTI-FOG KIT, 100-302-00?

The FDA product code for ENDOSCOPIC ANTI-FOG KIT, 100-302-00 is GCJ.

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Other records listing Avail-Southwest Division 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.

K952678STA-CLEAR ALCOHOL-FREE ENDOSCOPIC ANTI-FOG KITK950830STA-PUT NON-MAGNETIC INSTRUMENT DRAPE CATALOG #100-187-00 (16X20), 100-186-00 (16X10), 100-183-00 W/DEXTER WRAPK864158THERMAPAD

Related Devices (Code: GCJ)

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.

K262397CuratOR EX2742Eizo CorporationK260884UNIDRIVE Select SystemKarl Storz SE & CO. KGK260972OEV-271MUH LCD Monitor;OEV-321MUH LCD Monitor;OEV-431MUH LCD MonitorSony CorporationK261139VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)Freyja Healthcare, LLCK253541EZ-Close™ (EZ Close Port Site Closing Device, EZ Close MAX Port Site Closing Device, EZ Close II Port Site Closing Device)Medical ImpactK261614LED LCD Monitor (OEV-271H)Lg Electronics.Inc

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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