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FDA 510(k)

JENNINGS JAVELIN

K-Number: K942548 · 1994-11-03

ApplicantJfi Endineering, Inc.
Decision Date1994-11-03
Product CodeFMK
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

JENNINGS JAVELIN is the device name listed in this FDA 510(k) record. The listed applicant is Jfi Endineering, Inc.. It received FDA 510(k) clearance on 1994-11-03 under 510(k) number K942548. 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 JENNINGS JAVELIN?

JENNINGS JAVELIN is a medical device that received FDA 510(k) clearance on 1994-11-03. The listed applicant is Jfi Endineering, Inc.. The 510(k) number is K942548.

When did JENNINGS JAVELIN receive FDA 510(k) clearance?

JENNINGS JAVELIN received FDA 510(k) clearance on 1994-11-03, under 510(k) number K942548.

Who is the listed applicant for JENNINGS JAVELIN?

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

What is the FDA product code for JENNINGS JAVELIN?

The FDA product code for JENNINGS JAVELIN 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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