OPERATING SCISSORS 4 & 1/2 BLUNT/BLUNT
K-Number: K821119 · 1982-05-07
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Device Summary
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.
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
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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