INJECTRITE-C15 AND INJECTRITE-C30
K-Number: K002127 · 2000-12-29
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Device Summary
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.
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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