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FDA 510(k)

INJECTRITE-C15 AND INJECTRITE-C30

K-Number: K002127 · 2000-12-29

Decision Date2000-12-29
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INJECTRITE-C15 AND INJECTRITE-C30 is the device name listed in this FDA 510(k) record. The listed applicant is Sterling Medivations, Inc.. It received FDA 510(k) clearance on 2000-12-29 under 510(k) number K002127. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INJECTRITE-C15 AND INJECTRITE-C30?

INJECTRITE-C15 AND INJECTRITE-C30 is a medical device that received FDA 510(k) clearance on 2000-12-29. The listed applicant is Sterling Medivations, Inc.. The 510(k) number is K002127.

When did INJECTRITE-C15 AND INJECTRITE-C30 receive FDA 510(k) clearance?

INJECTRITE-C15 AND INJECTRITE-C30 received FDA 510(k) clearance on 2000-12-29, under 510(k) number K002127.

Who is the listed applicant for INJECTRITE-C15 AND INJECTRITE-C30?

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

What is the FDA product code for INJECTRITE-C15 AND INJECTRITE-C30?

The FDA product code for INJECTRITE-C15 AND INJECTRITE-C30 is FMF.

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 Sterling Medivations, 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.

View all 27 devices →

Related Devices (Code: FMF)

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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