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)

PEDIATRIC VENTILATOR CIRCUIT 2C7131

K-Number: K813155 · 1981-12-09

Decision Date1981-12-09
Product CodeBZO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PEDIATRIC VENTILATOR CIRCUIT 2C7131 is the device name listed in this FDA 510(k) record. The listed applicant is Travenol Laboratories, S.A.. It received FDA 510(k) clearance on 1981-12-09 under 510(k) number K813155. The device is classified under product code BZO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEDIATRIC VENTILATOR CIRCUIT 2C7131?

PEDIATRIC VENTILATOR CIRCUIT 2C7131 is a medical device that received FDA 510(k) clearance on 1981-12-09. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K813155.

When did PEDIATRIC VENTILATOR CIRCUIT 2C7131 receive FDA 510(k) clearance?

PEDIATRIC VENTILATOR CIRCUIT 2C7131 received FDA 510(k) clearance on 1981-12-09, under 510(k) number K813155.

Who is the listed applicant for PEDIATRIC VENTILATOR CIRCUIT 2C7131?

The FDA 510(k) record lists Travenol Laboratories, S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PEDIATRIC VENTILATOR CIRCUIT 2C7131?

The FDA product code for PEDIATRIC VENTILATOR CIRCUIT 2C7131 is BZO.

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 Travenol Laboratories, S.A. 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 206 devices →

Related Devices (Code: BZO)

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.

↑