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)

VOLUMETRIC PUMP CASSETTE W/ATTACHED SET

K-Number: K820860 · 1982-04-21

Decision Date1982-04-21
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VOLUMETRIC PUMP CASSETTE W/ATTACHED SET 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 1982-04-21 under 510(k) number K820860. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VOLUMETRIC PUMP CASSETTE W/ATTACHED SET?

VOLUMETRIC PUMP CASSETTE W/ATTACHED SET is a medical device that received FDA 510(k) clearance on 1982-04-21. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K820860.

When did VOLUMETRIC PUMP CASSETTE W/ATTACHED SET receive FDA 510(k) clearance?

VOLUMETRIC PUMP CASSETTE W/ATTACHED SET received FDA 510(k) clearance on 1982-04-21, under 510(k) number K820860.

Who is the listed applicant for VOLUMETRIC PUMP CASSETTE W/ATTACHED SET?

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 VOLUMETRIC PUMP CASSETTE W/ATTACHED SET?

The FDA product code for VOLUMETRIC PUMP CASSETTE W/ATTACHED SET is FRN.

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: FRN)

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.

↑