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FDA 510(k)

CENTAURSET 300 & 300 P.E.D

K-Number: K830258 · 1983-02-15

Decision Date1983-02-15
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CENTAURSET 300 & 300 P.E.D is the device name listed in this FDA 510(k) record. The listed applicant is Centaur Sciences, Inc.. It received FDA 510(k) clearance on 1983-02-15 under 510(k) number K830258. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTAURSET 300 & 300 P.E.D?

CENTAURSET 300 & 300 P.E.D is a medical device that received FDA 510(k) clearance on 1983-02-15. The listed applicant is Centaur Sciences, Inc.. The 510(k) number is K830258.

When did CENTAURSET 300 & 300 P.E.D receive FDA 510(k) clearance?

CENTAURSET 300 & 300 P.E.D received FDA 510(k) clearance on 1983-02-15, under 510(k) number K830258.

Who is the listed applicant for CENTAURSET 300 & 300 P.E.D?

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

What is the FDA product code for CENTAURSET 300 & 300 P.E.D?

The FDA product code for CENTAURSET 300 & 300 P.E.D is FPA.

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 Centaur Sciences, 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: FPA)

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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