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FDA 510(k)

BIOPSY FORCEP (NON-ELECTRIC)

K-Number: K896147 · 1990-04-16

ApplicantPortlyn Corp.
Decision Date1990-04-16
Product CodeFCL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BIOPSY FORCEP (NON-ELECTRIC) is the device name listed in this FDA 510(k) record. The listed applicant is Portlyn Corp.. It received FDA 510(k) clearance on 1990-04-16 under 510(k) number K896147. The device is classified under product code FCL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 8 devices →

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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