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)

MULTICHEM ALBUMIN REAGENT S0902

K-Number: K874049 · 1987-10-29

ApplicantSimmler, Inc.
Decision Date1987-10-29
Product CodeCIX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MULTICHEM ALBUMIN REAGENT S0902 is the device name listed in this FDA 510(k) record. The listed applicant is Simmler, Inc.. It received FDA 510(k) clearance on 1987-10-29 under 510(k) number K874049. The device is classified under product code CIX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTICHEM ALBUMIN REAGENT S0902?

MULTICHEM ALBUMIN REAGENT S0902 is a medical device that received FDA 510(k) clearance on 1987-10-29. The listed applicant is Simmler, Inc.. The 510(k) number is K874049.

When did MULTICHEM ALBUMIN REAGENT S0902 receive FDA 510(k) clearance?

MULTICHEM ALBUMIN REAGENT S0902 received FDA 510(k) clearance on 1987-10-29, under 510(k) number K874049.

Who is the listed applicant for MULTICHEM ALBUMIN REAGENT S0902?

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

What is the FDA product code for MULTICHEM ALBUMIN REAGENT S0902?

The FDA product code for MULTICHEM ALBUMIN REAGENT S0902 is CIX.

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 Simmler, 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 23 devices →

Related Devices (Code: CIX)

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.

↑