OLYMPUS BIOPSY FORCEPS MODEL FB-44
K-Number: K950786 · 1995-03-06
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Device Summary
Frequently Asked Questions
What is the OLYMPUS BIOPSY FORCEPS MODEL FB-44?
OLYMPUS BIOPSY FORCEPS MODEL FB-44 is a medical device that received FDA 510(k) clearance on 1995-03-06. The listed applicant is Olympus America, Inc.. The 510(k) number is K950786.
When did OLYMPUS BIOPSY FORCEPS MODEL FB-44 receive FDA 510(k) clearance?
OLYMPUS BIOPSY FORCEPS MODEL FB-44 received FDA 510(k) clearance on 1995-03-06, under 510(k) number K950786.
Who is the listed applicant for OLYMPUS BIOPSY FORCEPS MODEL FB-44?
The FDA 510(k) record lists Olympus America, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OLYMPUS BIOPSY FORCEPS MODEL FB-44?
The FDA product code for OLYMPUS BIOPSY FORCEPS MODEL FB-44 is EOQ.
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 Olympus America, 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: EOQ)
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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