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)

ACETAMINOPHEN/SALICYLATE CONTROL

K-Number: K810235 · 1981-02-10

Decision Date1981-02-10
Product CodeDIF
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

ACETAMINOPHEN/SALICYLATE CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Clin Tech Diagnostics Corp.. It received FDA 510(k) clearance on 1981-02-10 under 510(k) number K810235. The device is classified under product code DIF. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACETAMINOPHEN/SALICYLATE CONTROL?

ACETAMINOPHEN/SALICYLATE CONTROL is a medical device that received FDA 510(k) clearance on 1981-02-10. The listed applicant is Clin Tech Diagnostics Corp.. The 510(k) number is K810235.

When did ACETAMINOPHEN/SALICYLATE CONTROL receive FDA 510(k) clearance?

ACETAMINOPHEN/SALICYLATE CONTROL received FDA 510(k) clearance on 1981-02-10, under 510(k) number K810235.

Who is the listed applicant for ACETAMINOPHEN/SALICYLATE CONTROL?

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

What is the FDA product code for ACETAMINOPHEN/SALICYLATE CONTROL?

The FDA product code for ACETAMINOPHEN/SALICYLATE CONTROL is DIF.

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 Clin Tech Diagnostics 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.

Related Devices (Code: DIF)

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.

↑