Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CONPHAR SURGICAL RAZORR

K-Number: K791798 · 1980-02-01

ApplicantConphar, Inc.
Decision Date1980-02-01
Product CodeLDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CONPHAR SURGICAL RAZORR is the device name listed in this FDA 510(k) record. The listed applicant is Conphar, Inc.. It received FDA 510(k) clearance on 1980-02-01 under 510(k) number K791798. The device is classified under product code LDQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 122 devices →

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.

↑