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FDA 510(k)

OPERATING SCISSORS 4 & 1/2 BLUNT/BLUNT

K-Number: K821119 · 1982-05-07

ApplicantConphar, Inc.
Decision Date1982-05-07
Product CodeFZT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

OPERATING SCISSORS 4 & 1/2 BLUNT/BLUNT is the device name listed in this FDA 510(k) record. The listed applicant is Conphar, Inc.. It received FDA 510(k) clearance on 1982-05-07 under 510(k) number K821119. 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 OPERATING SCISSORS 4 & 1/2 BLUNT/BLUNT?

OPERATING SCISSORS 4 & 1/2 BLUNT/BLUNT is a medical device that received FDA 510(k) clearance on 1982-05-07. The listed applicant is Conphar, Inc.. The 510(k) number is K821119.

When did OPERATING SCISSORS 4 & 1/2 BLUNT/BLUNT receive FDA 510(k) clearance?

OPERATING SCISSORS 4 & 1/2 BLUNT/BLUNT received FDA 510(k) clearance on 1982-05-07, under 510(k) number K821119.

Who is the listed applicant for OPERATING SCISSORS 4 & 1/2 BLUNT/BLUNT?

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 OPERATING SCISSORS 4 & 1/2 BLUNT/BLUNT?

The FDA product code for OPERATING SCISSORS 4 & 1/2 BLUNT/BLUNT 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.

View all 122 devices →

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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