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FDA 510(k)

MEDIUM 199 W/EARLE'S SALTS & GLUTAMINE

K-Number: K810772 · 1981-05-13

ApplicantDutchland Laboratories, Inc.
Decision Date1981-05-13
Product CodeKIT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

MEDIUM 199 W/EARLE'S SALTS & GLUTAMINE is the device name listed in this FDA 510(k) record. The listed applicant is Dutchland Laboratories, Inc.. It received FDA 510(k) clearance on 1981-05-13 under 510(k) number K810772. The device is classified under product code KIT. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDIUM 199 W/EARLE'S SALTS & GLUTAMINE?

MEDIUM 199 W/EARLE'S SALTS & GLUTAMINE is a medical device that received FDA 510(k) clearance on 1981-05-13. The listed applicant is Dutchland Laboratories, Inc.. The 510(k) number is K810772.

When did MEDIUM 199 W/EARLE'S SALTS & GLUTAMINE receive FDA 510(k) clearance?

MEDIUM 199 W/EARLE'S SALTS & GLUTAMINE received FDA 510(k) clearance on 1981-05-13, under 510(k) number K810772.

Who is the listed applicant for MEDIUM 199 W/EARLE'S SALTS & GLUTAMINE?

The FDA 510(k) record lists Dutchland Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDIUM 199 W/EARLE'S SALTS & GLUTAMINE?

The FDA product code for MEDIUM 199 W/EARLE'S SALTS & GLUTAMINE is KIT.

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Related Devices (Code: KIT)

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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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