CONPHAR IRIS SCISSORS
K-Number: K821352 · 1982-05-27
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Device Summary
Frequently Asked Questions
What is the CONPHAR IRIS SCISSORS?
CONPHAR IRIS 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 K821352.
When did CONPHAR IRIS SCISSORS receive FDA 510(k) clearance?
CONPHAR IRIS SCISSORS received FDA 510(k) clearance on 1982-05-27, under 510(k) number K821352.
Who is the listed applicant for CONPHAR IRIS 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 IRIS SCISSORS?
The FDA product code for CONPHAR IRIS 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.
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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