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FDA 510(k)

CONPHAR DISSECTING SCISSORS

K-Number: K821351 · 1982-05-27

ApplicantConphar, Inc.
Decision Date1982-05-27
Product CodeFZT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CONPHAR DISSECTING SCISSORS is the device name listed in this FDA 510(k) record. The listed applicant is Conphar, Inc.. It received FDA 510(k) clearance on 1982-05-27 under 510(k) number K821351. The device is classified under product code FZT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONPHAR DISSECTING SCISSORS?

CONPHAR DISSECTING SCISSORS is a medical device that received FDA 510(k) clearance on 1982-05-27. The listed applicant is Conphar, Inc.. The 510(k) number is K821351.

When did CONPHAR DISSECTING SCISSORS receive FDA 510(k) clearance?

CONPHAR DISSECTING SCISSORS received FDA 510(k) clearance on 1982-05-27, under 510(k) number K821351.

Who is the listed applicant for CONPHAR DISSECTING SCISSORS?

The FDA 510(k) record lists Conphar, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONPHAR DISSECTING SCISSORS?

The FDA product code for CONPHAR DISSECTING SCISSORS is FZT.

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 Conphar, 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.

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Related Devices (Code: FZT)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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