FLEXIBLE BIOPSY FORCEP
K-Number: K871809 · 1987-06-18
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Device Summary
Frequently Asked Questions
What is the FLEXIBLE BIOPSY FORCEP?
FLEXIBLE BIOPSY FORCEP is a medical device that received FDA 510(k) clearance on 1987-06-18. The listed applicant is Surgi-Aid Endoscopics, Inc.. The 510(k) number is K871809.
When did FLEXIBLE BIOPSY FORCEP receive FDA 510(k) clearance?
FLEXIBLE BIOPSY FORCEP received FDA 510(k) clearance on 1987-06-18, under 510(k) number K871809.
Who is the listed applicant for FLEXIBLE BIOPSY FORCEP?
The FDA 510(k) record lists Surgi-Aid Endoscopics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLEXIBLE BIOPSY FORCEP?
The FDA product code for FLEXIBLE BIOPSY FORCEP 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.
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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