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FDA 510(k)

ADVANCED SURGICAL, INC. CANNULA CLEANING DEVICE AND ACCESSORIES

K-Number: K933812 · 1993-12-13

Decision Date1993-12-13
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ADVANCED SURGICAL, INC. CANNULA CLEANING DEVICE AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Surgical, Inc.. It received FDA 510(k) clearance on 1993-12-13 under 510(k) number K933812. 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 ADVANCED SURGICAL, INC. CANNULA CLEANING DEVICE AND ACCESSORIES?

ADVANCED SURGICAL, INC. CANNULA CLEANING DEVICE AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1993-12-13. The listed applicant is Advanced Surgical, Inc.. The 510(k) number is K933812.

When did ADVANCED SURGICAL, INC. CANNULA CLEANING DEVICE AND ACCESSORIES receive FDA 510(k) clearance?

ADVANCED SURGICAL, INC. CANNULA CLEANING DEVICE AND ACCESSORIES received FDA 510(k) clearance on 1993-12-13, under 510(k) number K933812.

Who is the listed applicant for ADVANCED SURGICAL, INC. CANNULA CLEANING DEVICE AND ACCESSORIES?

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

What is the FDA product code for ADVANCED SURGICAL, INC. CANNULA CLEANING DEVICE AND ACCESSORIES?

The FDA product code for ADVANCED SURGICAL, INC. CANNULA CLEANING DEVICE AND ACCESSORIES is GCJ.

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.

Other records listing Advanced Surgical, Inc. 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.

View all 21 devices →

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.

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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