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)

3&4 WAY PLASTIC STOPCOCKS, NONSTERILE

K-Number: K792125 · 1980-01-16

Decision Date1980-01-16
Product CodeFMG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

3&4 WAY PLASTIC STOPCOCKS, NONSTERILE is the device name listed in this FDA 510(k) record. The listed applicant is Tronomed, Inc.. It received FDA 510(k) clearance on 1980-01-16 under 510(k) number K792125. The device is classified under product code FMG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 3&4 WAY PLASTIC STOPCOCKS, NONSTERILE?

3&4 WAY PLASTIC STOPCOCKS, NONSTERILE is a medical device that received FDA 510(k) clearance on 1980-01-16. The listed applicant is Tronomed, Inc.. The 510(k) number is K792125.

When did 3&4 WAY PLASTIC STOPCOCKS, NONSTERILE receive FDA 510(k) clearance?

3&4 WAY PLASTIC STOPCOCKS, NONSTERILE received FDA 510(k) clearance on 1980-01-16, under 510(k) number K792125.

Who is the listed applicant for 3&4 WAY PLASTIC STOPCOCKS, NONSTERILE?

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

What is the FDA product code for 3&4 WAY PLASTIC STOPCOCKS, NONSTERILE?

The FDA product code for 3&4 WAY PLASTIC STOPCOCKS, NONSTERILE is FMG.

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 Tronomed, 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 12 devices →

Related Devices (Code: FMG)

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.

↑