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FDA 510(k)

STA-CLEAR ALCOHOL-FREE ENDOSCOPIC ANTI-FOG KIT

K-Number: K952678 · 1995-07-10

ApplicantAvail-Southwest Division
Decision Date1995-07-10
Product CodeKDG
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STA-CLEAR ALCOHOL-FREE ENDOSCOPIC ANTI-FOG KIT 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 1995-07-10 under 510(k) number K952678. The device is classified under product code KDG. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STA-CLEAR ALCOHOL-FREE ENDOSCOPIC ANTI-FOG KIT?

STA-CLEAR ALCOHOL-FREE ENDOSCOPIC ANTI-FOG KIT is a medical device that received FDA 510(k) clearance on 1995-07-10. The listed applicant is Avail-Southwest Division. The 510(k) number is K952678.

When did STA-CLEAR ALCOHOL-FREE ENDOSCOPIC ANTI-FOG KIT receive FDA 510(k) clearance?

STA-CLEAR ALCOHOL-FREE ENDOSCOPIC ANTI-FOG KIT received FDA 510(k) clearance on 1995-07-10, under 510(k) number K952678.

Who is the listed applicant for STA-CLEAR ALCOHOL-FREE ENDOSCOPIC ANTI-FOG KIT?

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 STA-CLEAR ALCOHOL-FREE ENDOSCOPIC ANTI-FOG KIT?

The FDA product code for STA-CLEAR ALCOHOL-FREE ENDOSCOPIC ANTI-FOG KIT is KDG.

Related Clinical Trials

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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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.

K950830STA-PUT NON-MAGNETIC INSTRUMENT DRAPE CATALOG #100-187-00 (16X20), 100-186-00 (16X10), 100-183-00 W/DEXTER WRAPK933520ENDOSCOPIC ANTI-FOG KIT, 100-302-00K864158THERMAPAD

Related Devices (Code: KDG)

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.

K952200OMNI-JUGWaterstone Medical, Inc.K894785SURGICAL CHISEL/OSTEOTOMEFdt Precision Machine Co., Inc.K891471SIL-MED WASTE FLUID DUMP BAGSil-Med Corp.K872947POREX QUALITY PLASTIC SURGERY INSTRUMENTSPorex MedicalK872092OSTEOTOME SET, HOKE, STRAIGHT, SET OF 5Military Engineering, Inc.K842824CHERMEL BONE CHISELSCher Mel Corp.

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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