Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

URIC ACID TEST, BMC AUTOFLO

K-Number: K770272 · 1977-03-01

Decision Date1977-03-01
Product CodeKNK
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

URIC ACID TEST, BMC AUTOFLO 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 1977-03-01 under 510(k) number K770272. 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 TEST, BMC AUTOFLO?

URIC ACID TEST, BMC AUTOFLO is a medical device that received FDA 510(k) clearance on 1977-03-01. The listed applicant is Boehringer Mannheim Corp.. The 510(k) number is K770272.

When did URIC ACID TEST, BMC AUTOFLO receive FDA 510(k) clearance?

URIC ACID TEST, BMC AUTOFLO received FDA 510(k) clearance on 1977-03-01, under 510(k) number K770272.

Who is the listed applicant for URIC ACID TEST, BMC AUTOFLO?

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 TEST, BMC AUTOFLO?

The FDA product code for URIC ACID TEST, BMC AUTOFLO is KNK.

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 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

View on FDA Database →

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

↑