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FDA 510(k)

BASAL MEDIUM EAGLE W/HANKS' SALTS

K-Number: K810773 · 1981-05-13

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

Device Summary

BASAL MEDIUM EAGLE W/HANKS' SALTS 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 K810773. 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 BASAL MEDIUM EAGLE W/HANKS' SALTS?

BASAL MEDIUM EAGLE W/HANKS' SALTS 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 K810773.

When did BASAL MEDIUM EAGLE W/HANKS' SALTS receive FDA 510(k) clearance?

BASAL MEDIUM EAGLE W/HANKS' SALTS received FDA 510(k) clearance on 1981-05-13, under 510(k) number K810773.

Who is the listed applicant for BASAL MEDIUM EAGLE W/HANKS' SALTS?

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 BASAL MEDIUM EAGLE W/HANKS' SALTS?

The FDA product code for BASAL MEDIUM EAGLE W/HANKS' SALTS 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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