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FDA 510(k)

QB II BLUNT DISSECTOR

K-Number: K933604 · 1993-09-23

ApplicantJoyce M. Shotwell, M.D.
Decision Date1993-09-23
Product CodeFGS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

QB II BLUNT DISSECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Joyce M. Shotwell, M.D.. It received FDA 510(k) clearance on 1993-09-23 under 510(k) number K933604. The device is classified under product code FGS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QB II BLUNT DISSECTOR?

QB II BLUNT DISSECTOR is a medical device that received FDA 510(k) clearance on 1993-09-23. The listed applicant is Joyce M. Shotwell, M.D.. The 510(k) number is K933604.

When did QB II BLUNT DISSECTOR receive FDA 510(k) clearance?

QB II BLUNT DISSECTOR received FDA 510(k) clearance on 1993-09-23, under 510(k) number K933604.

Who is the listed applicant for QB II BLUNT DISSECTOR?

The FDA 510(k) record lists Joyce M. Shotwell, M.D. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QB II BLUNT DISSECTOR?

The FDA product code for QB II BLUNT DISSECTOR is FGS.

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Related Devices (Code: FGS)

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.

K931854ENDOSCOPIC BLUNT DISSECTING INSTRUMENTMayaguez Medical CenterK923818O.R. CONCEPTS' IRRIGATING KITTNERO.R. Concepts, Inc.K822194ENDOSCOPIC SPONGE CARRIERKelleher 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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