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FDA 510(k)

LAS-R TM

K-Number: K771780 · 1977-10-04

ApplicantHyland Therapeutic Div., Travenol Laboratories
Decision Date1977-10-04
Product CodeDEB
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

LAS-R TM is the device name listed in this FDA 510(k) record. The listed applicant is Hyland Therapeutic Div., Travenol Laboratories. It received FDA 510(k) clearance on 1977-10-04 under 510(k) number K771780. The device is classified under product code DEB. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAS-R TM?

LAS-R TM is a medical device that received FDA 510(k) clearance on 1977-10-04. The listed applicant is Hyland Therapeutic Div., Travenol Laboratories. The 510(k) number is K771780.

When did LAS-R TM receive FDA 510(k) clearance?

LAS-R TM received FDA 510(k) clearance on 1977-10-04, under 510(k) number K771780.

Who is the listed applicant for LAS-R TM?

The FDA 510(k) record lists Hyland Therapeutic Div., Travenol Laboratories as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LAS-R TM?

The FDA product code for LAS-R TM is DEB.

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Related Devices (Code: DEB)

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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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