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FDA 510(k)

MEDIKEEPER

K-Number: K912346 · 1991-07-30

ApplicantMedikeeper, Inc.
Decision Date1991-07-30
Product CodeBRY
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MEDIKEEPER is the device name listed in this FDA 510(k) record. The listed applicant is Medikeeper, Inc.. It received FDA 510(k) clearance on 1991-07-30 under 510(k) number K912346. The device is classified under product code BRY. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDIKEEPER?

MEDIKEEPER is a medical device that received FDA 510(k) clearance on 1991-07-30. The listed applicant is Medikeeper, Inc.. The 510(k) number is K912346.

When did MEDIKEEPER receive FDA 510(k) clearance?

MEDIKEEPER received FDA 510(k) clearance on 1991-07-30, under 510(k) number K912346.

Who is the listed applicant for MEDIKEEPER?

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

What is the FDA product code for MEDIKEEPER?

The FDA product code for MEDIKEEPER is BRY.

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Related Devices (Code: BRY)

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.

K921710MOVIT DEVICEJohn J. Navar, M.D.K901474ANESTHESIA WORKSTATIONSiemens Life Support SystemsK871564ANESTHASSISTAnestech, Inc.K821307ANESTHECACHEMed-Life, Inc.

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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