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FDA 510(k)

MINIMUM ESSENTIAL MEDIUM EAGLE W/EARLE

K-Number: K810769 · 1981-05-13

Decision Date1981-05-13
Product CodeKIT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

MINIMUM ESSENTIAL MEDIUM EAGLE W/EARLE 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 K810769. 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/EARLE?

MINIMUM ESSENTIAL MEDIUM EAGLE W/EARLE 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 K810769.

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

MINIMUM ESSENTIAL MEDIUM EAGLE W/EARLE received FDA 510(k) clearance on 1981-05-13, under 510(k) number K810769.

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

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/EARLE?

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

Related Clinical Trials

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.

Other records listing Dutchland Laboratories, Inc. as applicant

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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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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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