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 FACE MASK-STERILE

K-Number: K792110 · 1979-11-05

ApplicantConphar, Inc.
Decision Date1979-11-05
Product CodeFXX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CONPHAR FACE MASK-STERILE is the device name listed in this FDA 510(k) record. The listed applicant is Conphar, Inc.. It received FDA 510(k) clearance on 1979-11-05 under 510(k) number K792110. The device is classified under product code FXX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONPHAR FACE MASK-STERILE?

CONPHAR FACE MASK-STERILE is a medical device that received FDA 510(k) clearance on 1979-11-05. The listed applicant is Conphar, Inc.. The 510(k) number is K792110.

When did CONPHAR FACE MASK-STERILE receive FDA 510(k) clearance?

CONPHAR FACE MASK-STERILE received FDA 510(k) clearance on 1979-11-05, under 510(k) number K792110.

Who is the listed applicant for CONPHAR FACE MASK-STERILE?

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 FACE MASK-STERILE?

The FDA product code for CONPHAR FACE MASK-STERILE is FXX.

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: FXX)

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.

↑