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FDA 510(k)

HAM'S F-10-A SPEC. FORMULATION FROM DR. HAM

K-Number: K850515 · 1985-02-27

ApplicantMediatech, Inc.
Decision Date1985-02-27
Product CodeKIT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

HAM'S F-10-A SPEC. FORMULATION FROM DR. HAM is the device name listed in this FDA 510(k) record. The listed applicant is Mediatech, Inc.. It received FDA 510(k) clearance on 1985-02-27 under 510(k) number K850515. 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 HAM'S F-10-A SPEC. FORMULATION FROM DR. HAM?

HAM'S F-10-A SPEC. FORMULATION FROM DR. HAM is a medical device that received FDA 510(k) clearance on 1985-02-27. The listed applicant is Mediatech, Inc.. The 510(k) number is K850515.

When did HAM'S F-10-A SPEC. FORMULATION FROM DR. HAM receive FDA 510(k) clearance?

HAM'S F-10-A SPEC. FORMULATION FROM DR. HAM received FDA 510(k) clearance on 1985-02-27, under 510(k) number K850515.

Who is the listed applicant for HAM'S F-10-A SPEC. FORMULATION FROM DR. HAM?

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

What is the FDA product code for HAM'S F-10-A SPEC. FORMULATION FROM DR. HAM?

The FDA product code for HAM'S F-10-A SPEC. FORMULATION FROM DR. HAM 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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