BIOPSY FORCEP (NON-ELECTRIC)
K-Number: K896147 · 1990-04-16
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Device Summary
Frequently Asked Questions
What is the BIOPSY FORCEP (NON-ELECTRIC)?
BIOPSY FORCEP (NON-ELECTRIC) is a medical device that received FDA 510(k) clearance on 1990-04-16. The listed applicant is Portlyn Corp.. The 510(k) number is K896147.
When did BIOPSY FORCEP (NON-ELECTRIC) receive FDA 510(k) clearance?
BIOPSY FORCEP (NON-ELECTRIC) received FDA 510(k) clearance on 1990-04-16, under 510(k) number K896147.
Who is the listed applicant for BIOPSY FORCEP (NON-ELECTRIC)?
The FDA 510(k) record lists Portlyn Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BIOPSY FORCEP (NON-ELECTRIC)?
The FDA product code for BIOPSY FORCEP (NON-ELECTRIC) is FCL.
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 Portlyn Corp. 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: FCL)
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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