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FDA 510(k)

FREE-LANCE

K-Number: K944948 · 1994-11-17

ApplicantF.F.F. Enterprises, Inc.
Decision Date1994-11-17
Product CodeFMK
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FREE-LANCE is the device name listed in this FDA 510(k) record. The listed applicant is F.F.F. Enterprises, Inc.. It received FDA 510(k) clearance on 1994-11-17 under 510(k) number K944948. The device is classified under product code FMK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FREE-LANCE?

FREE-LANCE is a medical device that received FDA 510(k) clearance on 1994-11-17. The listed applicant is F.F.F. Enterprises, Inc.. The 510(k) number is K944948.

When did FREE-LANCE receive FDA 510(k) clearance?

FREE-LANCE received FDA 510(k) clearance on 1994-11-17, under 510(k) number K944948.

Who is the listed applicant for FREE-LANCE?

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

What is the FDA product code for FREE-LANCE?

The FDA product code for FREE-LANCE is FMK.

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Related Devices (Code: FMK)

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

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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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