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)

MICRO-BUMINTEST REAGENT TABLETS

K-Number: K874909 · 1988-04-28

Decision Date1988-04-28
Product CodeJIR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MICRO-BUMINTEST REAGENT TABLETS is the device name listed in this FDA 510(k) record. The listed applicant is Miles Laboratories, Inc.. It received FDA 510(k) clearance on 1988-04-28 under 510(k) number K874909. The device is classified under product code JIR. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO-BUMINTEST REAGENT TABLETS?

MICRO-BUMINTEST REAGENT TABLETS is a medical device that received FDA 510(k) clearance on 1988-04-28. The listed applicant is Miles Laboratories, Inc.. The 510(k) number is K874909.

When did MICRO-BUMINTEST REAGENT TABLETS receive FDA 510(k) clearance?

MICRO-BUMINTEST REAGENT TABLETS received FDA 510(k) clearance on 1988-04-28, under 510(k) number K874909.

Who is the listed applicant for MICRO-BUMINTEST REAGENT TABLETS?

The FDA 510(k) record lists Miles Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICRO-BUMINTEST REAGENT TABLETS?

The FDA product code for MICRO-BUMINTEST REAGENT TABLETS is JIR.

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 Miles Laboratories, 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.

View all 158 devices →

Related Devices (Code: JIR)

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.

↑