ROUND CUP HOT BIOPSY FORCEP (MODEL D-52)
K-Number: K874010 · 1987-12-29
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Device Summary
Frequently Asked Questions
What is the ROUND CUP HOT BIOPSY FORCEP (MODEL D-52)?
ROUND CUP HOT BIOPSY FORCEP (MODEL D-52) is a medical device that received FDA 510(k) clearance on 1987-12-29. The listed applicant is Endovations. The 510(k) number is K874010.
When did ROUND CUP HOT BIOPSY FORCEP (MODEL D-52) receive FDA 510(k) clearance?
ROUND CUP HOT BIOPSY FORCEP (MODEL D-52) received FDA 510(k) clearance on 1987-12-29, under 510(k) number K874010.
Who is the listed applicant for ROUND CUP HOT BIOPSY FORCEP (MODEL D-52)?
The FDA 510(k) record lists Endovations as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ROUND CUP HOT BIOPSY FORCEP (MODEL D-52)?
The FDA product code for ROUND CUP HOT BIOPSY FORCEP (MODEL D-52) is OCZ.
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 Endovations 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: OCZ)
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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