ALCIDE REN NEW-D
K-Number: K844734 · 1985-05-17
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Device Summary
Frequently Asked Questions
What is the ALCIDE REN NEW-D?
ALCIDE REN NEW-D is a medical device that received FDA 510(k) clearance on 1985-05-17. The listed applicant is Alcide Corp.. The 510(k) number is K844734.
When did ALCIDE REN NEW-D receive FDA 510(k) clearance?
ALCIDE REN NEW-D received FDA 510(k) clearance on 1985-05-17, under 510(k) number K844734.
Who is the listed applicant for ALCIDE REN NEW-D?
The FDA 510(k) record lists Alcide Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALCIDE REN NEW-D?
The FDA product code for ALCIDE REN NEW-D is FKQ.
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 Alcide Corp. 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: FKQ)
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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