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)

CONDUCTIVE ANESTHSIA BREATH. CIRCUIT

K-Number: K760149 · 1976-07-19

Decision Date1976-07-19
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CONDUCTIVE ANESTHSIA BREATH. CIRCUIT is the device name listed in this FDA 510(k) record. The listed applicant is Omnicon Medical Corp.. It received FDA 510(k) clearance on 1976-07-19 under 510(k) number K760149. The device is classified under product code CAI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONDUCTIVE ANESTHSIA BREATH. CIRCUIT?

CONDUCTIVE ANESTHSIA BREATH. CIRCUIT is a medical device that received FDA 510(k) clearance on 1976-07-19. The listed applicant is Omnicon Medical Corp.. The 510(k) number is K760149.

When did CONDUCTIVE ANESTHSIA BREATH. CIRCUIT receive FDA 510(k) clearance?

CONDUCTIVE ANESTHSIA BREATH. CIRCUIT received FDA 510(k) clearance on 1976-07-19, under 510(k) number K760149.

Who is the listed applicant for CONDUCTIVE ANESTHSIA BREATH. CIRCUIT?

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

What is the FDA product code for CONDUCTIVE ANESTHSIA BREATH. CIRCUIT?

The FDA product code for CONDUCTIVE ANESTHSIA BREATH. CIRCUIT is CAI.

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 Omnicon Medical 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.

View all 10 devices →

Related Devices (Code: CAI)

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.

↑