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FDA 510(k)

LAS-R TEST PROGRAM

K-Number: K771226 · 1977-07-21

ApplicantHyland Therapeutic Div., Travenol Laboratories
Decision Date1977-07-21
Product CodeCFN
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

LAS-R TEST PROGRAM 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 1977-07-21 under 510(k) number K771226. The device is classified under product code CFN. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAS-R TEST PROGRAM?

LAS-R TEST PROGRAM is a medical device that received FDA 510(k) clearance on 1977-07-21. The listed applicant is Hyland Therapeutic Div., Travenol Laboratories. The 510(k) number is K771226.

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

LAS-R TEST PROGRAM received FDA 510(k) clearance on 1977-07-21, under 510(k) number K771226.

Who is the listed applicant for LAS-R TEST PROGRAM?

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 TEST PROGRAM?

The FDA product code for LAS-R TEST PROGRAM is CFN.

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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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