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FDA 510(k)

INTRAVENOUS INFUSION PUMP, CODE 2M8015

K-Number: K800629 · 1980-05-14

ApplicantTravenol Laboratories, S.A.
Decision Date1980-05-14
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INTRAVENOUS INFUSION PUMP, CODE 2M8015 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 1980-05-14 under 510(k) number K800629. 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 INTRAVENOUS INFUSION PUMP, CODE 2M8015?

INTRAVENOUS INFUSION PUMP, CODE 2M8015 is a medical device that received FDA 510(k) clearance on 1980-05-14. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K800629.

When did INTRAVENOUS INFUSION PUMP, CODE 2M8015 receive FDA 510(k) clearance?

INTRAVENOUS INFUSION PUMP, CODE 2M8015 received FDA 510(k) clearance on 1980-05-14, under 510(k) number K800629.

Who is the listed applicant for INTRAVENOUS INFUSION PUMP, CODE 2M8015?

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 INTRAVENOUS INFUSION PUMP, CODE 2M8015?

The FDA product code for INTRAVENOUS INFUSION PUMP, CODE 2M8015 is FRN.

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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.

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