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)

VALVE ANESTHETIC

K-Number: K771892 · 1978-02-02

ApplicantPromed Corp.
Decision Date1978-02-02
Product CodeCAD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VALVE ANESTHETIC is the device name listed in this FDA 510(k) record. The listed applicant is Promed Corp.. It received FDA 510(k) clearance on 1978-02-02 under 510(k) number K771892. The device is classified under product code CAD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VALVE ANESTHETIC?

VALVE ANESTHETIC is a medical device that received FDA 510(k) clearance on 1978-02-02. The listed applicant is Promed Corp.. The 510(k) number is K771892.

When did VALVE ANESTHETIC receive FDA 510(k) clearance?

VALVE ANESTHETIC received FDA 510(k) clearance on 1978-02-02, under 510(k) number K771892.

Who is the listed applicant for VALVE ANESTHETIC?

The FDA 510(k) record lists Promed Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VALVE ANESTHETIC?

The FDA product code for VALVE ANESTHETIC is CAD.

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 Promed Corp. 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: CAD)

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.

↑