FDA 510(k)

MINI-MILL

K-Number: K914035 · 1992-03-02

Decision Date1992-03-02

Product CodeEMI

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

MINI-MILL is the device name listed in this FDA 510(k) record. The listed applicant is Biomedical Composites, Ltd.. It received FDA 510(k) clearance on 1992-03-02 under 510(k) number K914035. The device is classified under product code EMI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINI-MILL?

MINI-MILL is a medical device that received FDA 510(k) clearance on 1992-03-02. The listed applicant is Biomedical Composites, Ltd.. The 510(k) number is K914035.

When did MINI-MILL receive FDA 510(k) clearance?

MINI-MILL received FDA 510(k) clearance on 1992-03-02, under 510(k) number K914035.

Who is the listed applicant for MINI-MILL?

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

What is the FDA product code for MINI-MILL?

The FDA product code for MINI-MILL is EMI.

Other records listing Biomedical Composites, Ltd. 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.

K871312FIBREFLEX

Related Devices (Code: EMI)

K912989PLANUSTAR AND DENS NOBILIS DENTURE TEETHWilde-USA, Inc.K851716865/1 TO 875/3 VARIOUS TYPES OF DENTAL BONE FILESArtiberia K823676DISC NEEDLE SET #TX-8220Today'S Machining & Design, 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.