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FDA 510(k)

I.V. LEVER CLAMP

K-Number: K780481 · 1978-04-10

ApplicantTravenol Laboratories, S.A.
Decision Date1978-04-10
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

I.V. LEVER CLAMP 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 1978-04-10 under 510(k) number K780481. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the I.V. LEVER CLAMP?

I.V. LEVER CLAMP is a medical device that received FDA 510(k) clearance on 1978-04-10. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K780481.

When did I.V. LEVER CLAMP receive FDA 510(k) clearance?

I.V. LEVER CLAMP received FDA 510(k) clearance on 1978-04-10, under 510(k) number K780481.

Who is the listed applicant for I.V. LEVER CLAMP?

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 I.V. LEVER CLAMP?

The FDA product code for I.V. LEVER CLAMP is FPA.

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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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