EMPTY STERILE CARPUJECT
K-Number: K820164 · 1982-02-24
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Device Summary
Frequently Asked Questions
What is the EMPTY STERILE CARPUJECT?
EMPTY STERILE CARPUJECT is a medical device that received FDA 510(k) clearance on 1982-02-24. The listed applicant is Sterling Drug, Inc.. The 510(k) number is K820164.
When did EMPTY STERILE CARPUJECT receive FDA 510(k) clearance?
EMPTY STERILE CARPUJECT received FDA 510(k) clearance on 1982-02-24, under 510(k) number K820164.
Who is the listed applicant for EMPTY STERILE CARPUJECT?
The FDA 510(k) record lists Sterling Drug, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EMPTY STERILE CARPUJECT?
The FDA product code for EMPTY STERILE CARPUJECT 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 Drug, 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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