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)

2M8101 HEATED LIQUID LEVEL CONTROLLER

K-Number: K802144 · 1980-09-26

Decision Date1980-09-26
Product CodeBTT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

2M8101 HEATED LIQUID LEVEL CONTROLLER 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 1980-09-26 under 510(k) number K802144. The device is classified under product code BTT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 2M8101 HEATED LIQUID LEVEL CONTROLLER?

2M8101 HEATED LIQUID LEVEL CONTROLLER is a medical device that received FDA 510(k) clearance on 1980-09-26. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K802144.

When did 2M8101 HEATED LIQUID LEVEL CONTROLLER receive FDA 510(k) clearance?

2M8101 HEATED LIQUID LEVEL CONTROLLER received FDA 510(k) clearance on 1980-09-26, under 510(k) number K802144.

Who is the listed applicant for 2M8101 HEATED LIQUID LEVEL CONTROLLER?

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 2M8101 HEATED LIQUID LEVEL CONTROLLER?

The FDA product code for 2M8101 HEATED LIQUID LEVEL CONTROLLER is BTT.

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: BTT)

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.

↑