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FDA 510(k)

URIC ACID PAP

K-Number: K873363 · 1987-10-19

Decision Date1987-10-19
Product CodeKNK
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

URIC ACID PAP is the device name listed in this FDA 510(k) record. The listed applicant is Boehringer Mannheim Corp.. It received FDA 510(k) clearance on 1987-10-19 under 510(k) number K873363. The device is classified under product code KNK. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 340 devices →

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

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

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