BIOPSY CUP FORCEPS
K-Number: K930180 · 1994-02-03
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Device Summary
Frequently Asked Questions
What is the BIOPSY CUP FORCEPS?
BIOPSY CUP FORCEPS is a medical device that received FDA 510(k) clearance on 1994-02-03. The listed applicant is Surgical Technologies, Inc.. The 510(k) number is K930180.
When did BIOPSY CUP FORCEPS receive FDA 510(k) clearance?
BIOPSY CUP FORCEPS received FDA 510(k) clearance on 1994-02-03, under 510(k) number K930180.
Who is the listed applicant for BIOPSY CUP FORCEPS?
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 BIOPSY CUP FORCEPS?
The FDA product code for BIOPSY CUP FORCEPS 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 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.
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
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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