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FDA 510(k)

T-RX RETRIEVAL FORCEPS

K-Number: K970982 · 1997-05-09

ApplicantTri-Med Specialties, Inc.
Decision Date1997-05-09
Product CodeOCZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

T-RX RETRIEVAL FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Tri-Med Specialties, Inc.. It received FDA 510(k) clearance on 1997-05-09 under 510(k) number K970982. The device is classified under product code OCZ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the T-RX RETRIEVAL FORCEPS?

T-RX RETRIEVAL FORCEPS is a medical device that received FDA 510(k) clearance on 1997-05-09. The listed applicant is Tri-Med Specialties, Inc.. The 510(k) number is K970982.

When did T-RX RETRIEVAL FORCEPS receive FDA 510(k) clearance?

T-RX RETRIEVAL FORCEPS received FDA 510(k) clearance on 1997-05-09, under 510(k) number K970982.

Who is the listed applicant for T-RX RETRIEVAL FORCEPS?

The FDA 510(k) record lists Tri-Med Specialties, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for T-RX RETRIEVAL FORCEPS?

The FDA product code for T-RX RETRIEVAL FORCEPS is OCZ.

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Other records listing Tri-Med Specialties, Inc. as applicant

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Related Devices (Code: OCZ)

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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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