CONPHAR SURGICAL RAZORR
K-Number: K791798 · 1980-02-01
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Device Summary
Frequently Asked Questions
What is the CONPHAR SURGICAL RAZORR?
CONPHAR SURGICAL RAZORR is a medical device that received FDA 510(k) clearance on 1980-02-01. The listed applicant is Conphar, Inc.. The 510(k) number is K791798.
When did CONPHAR SURGICAL RAZORR receive FDA 510(k) clearance?
CONPHAR SURGICAL RAZORR received FDA 510(k) clearance on 1980-02-01, under 510(k) number K791798.
Who is the listed applicant for CONPHAR SURGICAL RAZORR?
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 SURGICAL RAZORR?
The FDA product code for CONPHAR SURGICAL RAZORR is LDQ.
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: LDQ)
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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