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FDA 510(k)

BLUNT DISSECTING SCISSORS

K-Number: K930464 · 1993-06-04

ApplicantSurgical Technologies, Inc.
Decision Date1993-06-04
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BLUNT DISSECTING SCISSORS is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Technologies, Inc.. It received FDA 510(k) clearance on 1993-06-04 under 510(k) number K930464. 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 BLUNT DISSECTING SCISSORS?

BLUNT DISSECTING SCISSORS is a medical device that received FDA 510(k) clearance on 1993-06-04. The listed applicant is Surgical Technologies, Inc.. The 510(k) number is K930464.

When did BLUNT DISSECTING SCISSORS receive FDA 510(k) clearance?

BLUNT DISSECTING SCISSORS received FDA 510(k) clearance on 1993-06-04, under 510(k) number K930464.

Who is the listed applicant for BLUNT DISSECTING SCISSORS?

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

What is the FDA product code for BLUNT DISSECTING SCISSORS?

The FDA product code for BLUNT DISSECTING SCISSORS is GCJ.

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Other records listing Surgical Technologies, 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.

K941992CYSTOSCOPEK942029ARTHROSCOPEK946136INFINITECH LIGHTED INFUSION CANNULAK952566OSCILFLATORK951918SURGICAL TECHNOLOGIES, INC. SYRINGEK950683ARTHROGRAM TRAY

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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.

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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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