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)

SERUM ALCOHOL CONTROL LEVELS 1, 2 & 3

K-Number: K912827 · 1991-08-12

Decision Date1991-08-12
Product CodeDKC
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

SERUM ALCOHOL CONTROL LEVELS 1, 2 & 3 is the device name listed in this FDA 510(k) record. The listed applicant is Cala Diagnostics. It received FDA 510(k) clearance on 1991-08-12 under 510(k) number K912827. The device is classified under product code DKC. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SERUM ALCOHOL CONTROL LEVELS 1, 2 & 3?

SERUM ALCOHOL CONTROL LEVELS 1, 2 & 3 is a medical device that received FDA 510(k) clearance on 1991-08-12. The listed applicant is Cala Diagnostics. The 510(k) number is K912827.

When did SERUM ALCOHOL CONTROL LEVELS 1, 2 & 3 receive FDA 510(k) clearance?

SERUM ALCOHOL CONTROL LEVELS 1, 2 & 3 received FDA 510(k) clearance on 1991-08-12, under 510(k) number K912827.

Who is the listed applicant for SERUM ALCOHOL CONTROL LEVELS 1, 2 & 3?

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

What is the FDA product code for SERUM ALCOHOL CONTROL LEVELS 1, 2 & 3?

The FDA product code for SERUM ALCOHOL CONTROL LEVELS 1, 2 & 3 is DKC.

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 Cala Diagnostics 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 12 devices →

Related Devices (Code: DKC)

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.

↑