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FDA 510(k)

DOSE RELEASE OF STERILIZATION LOTS

K-Number: K841949 · 1984-09-05

Decision Date1984-09-05
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DOSE RELEASE OF STERILIZATION LOTS is the device name listed in this FDA 510(k) record. The listed applicant is Medcare Disp Products, Inc.. It received FDA 510(k) clearance on 1984-09-05 under 510(k) number K841949. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DOSE RELEASE OF STERILIZATION LOTS?

DOSE RELEASE OF STERILIZATION LOTS is a medical device that received FDA 510(k) clearance on 1984-09-05. The listed applicant is Medcare Disp Products, Inc.. The 510(k) number is K841949.

When did DOSE RELEASE OF STERILIZATION LOTS receive FDA 510(k) clearance?

DOSE RELEASE OF STERILIZATION LOTS received FDA 510(k) clearance on 1984-09-05, under 510(k) number K841949.

Who is the listed applicant for DOSE RELEASE OF STERILIZATION LOTS?

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

What is the FDA product code for DOSE RELEASE OF STERILIZATION LOTS?

The FDA product code for DOSE RELEASE OF STERILIZATION LOTS is FMF.

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 Medcare Disp Products, 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.

Related Devices (Code: FMF)

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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