FDA 510(k)

EARLE'S MEM W/NON-ESSENTIAL AMINO ACIDS POWDER MED

K-Number: K850223 · 1985-03-07

ApplicantHazleton Research Products, Inc.

Decision Date1985-03-07

Product CodeKIT

Advisory CommitteeHE

DecisionSubstantially Equivalent

Device Summary

EARLE'S MEM W/NON-ESSENTIAL AMINO ACIDS POWDER MED is the device name listed in this FDA 510(k) record. The listed applicant is Hazleton Research Products, Inc.. It received FDA 510(k) clearance on 1985-03-07 under 510(k) number K850223. 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 EARLE'S MEM W/NON-ESSENTIAL AMINO ACIDS POWDER MED?

EARLE'S MEM W/NON-ESSENTIAL AMINO ACIDS POWDER MED is a medical device that received FDA 510(k) clearance on 1985-03-07. The listed applicant is Hazleton Research Products, Inc.. The 510(k) number is K850223.

When did EARLE'S MEM W/NON-ESSENTIAL AMINO ACIDS POWDER MED receive FDA 510(k) clearance?

EARLE'S MEM W/NON-ESSENTIAL AMINO ACIDS POWDER MED received FDA 510(k) clearance on 1985-03-07, under 510(k) number K850223.

Who is the listed applicant for EARLE'S MEM W/NON-ESSENTIAL AMINO ACIDS POWDER MED?

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

What is the FDA product code for EARLE'S MEM W/NON-ESSENTIAL AMINO ACIDS POWDER MED?

The FDA product code for EARLE'S MEM W/NON-ESSENTIAL AMINO ACIDS POWDER MED is KIT.

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Other records listing Hazleton Research Products, Inc. as applicant

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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.