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FDA 510(k)

MINIMUM ESSENTIAL MEDIUM EAGLE W/HANKS

K-Number: K810768 · 1981-05-13

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

Device Summary

MINIMUM ESSENTIAL MEDIUM EAGLE W/HANKS 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 K810768. 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 MINIMUM ESSENTIAL MEDIUM EAGLE W/HANKS?

MINIMUM ESSENTIAL MEDIUM EAGLE W/HANKS 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 K810768.

When did MINIMUM ESSENTIAL MEDIUM EAGLE W/HANKS receive FDA 510(k) clearance?

MINIMUM ESSENTIAL MEDIUM EAGLE W/HANKS received FDA 510(k) clearance on 1981-05-13, under 510(k) number K810768.

Who is the listed applicant for MINIMUM ESSENTIAL MEDIUM EAGLE W/HANKS?

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 MINIMUM ESSENTIAL MEDIUM EAGLE W/HANKS?

The FDA product code for MINIMUM ESSENTIAL MEDIUM EAGLE W/HANKS is KIT.

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Related Devices (Code: KIT)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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