URIC ACID PAP
K-Number: K873363 · 1987-10-19
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Device Summary
Frequently Asked Questions
What is the URIC ACID PAP?
URIC ACID PAP is a medical device that received FDA 510(k) clearance on 1987-10-19. The listed applicant is Boehringer Mannheim Corp.. The 510(k) number is K873363.
When did URIC ACID PAP receive FDA 510(k) clearance?
URIC ACID PAP received FDA 510(k) clearance on 1987-10-19, under 510(k) number K873363.
Who is the listed applicant for URIC ACID PAP?
The FDA 510(k) record lists Boehringer Mannheim Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for URIC ACID PAP?
The FDA product code for URIC ACID PAP is KNK.
Other records listing Boehringer Mannheim 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: KNK)
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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