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FDA 510(k)

MANGAR BOOSTER

K-Number: K905414 · 1991-03-05

ApplicantNorthfleet Management Group, Inc.
Decision Date1991-03-05
Product CodeFNG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MANGAR BOOSTER is the device name listed in this FDA 510(k) record. The listed applicant is Northfleet Management Group, Inc.. It received FDA 510(k) clearance on 1991-03-05 under 510(k) number K905414. The device is classified under product code FNG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MANGAR BOOSTER?

MANGAR BOOSTER is a medical device that received FDA 510(k) clearance on 1991-03-05. The listed applicant is Northfleet Management Group, Inc.. The 510(k) number is K905414.

When did MANGAR BOOSTER receive FDA 510(k) clearance?

MANGAR BOOSTER received FDA 510(k) clearance on 1991-03-05, under 510(k) number K905414.

Who is the listed applicant for MANGAR BOOSTER?

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

What is the FDA product code for MANGAR BOOSTER?

The FDA product code for MANGAR BOOSTER is FNG.

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Related Devices (Code: FNG)

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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