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)

ONE TIME ACETONE/ALCOHOL;SWAB STICKS

K-Number: K833141 · 1983-10-31

Decision Date1983-10-31
Product CodeLKB
DecisionSubstantially Equivalent

Device Summary

ONE TIME ACETONE/ALCOHOL;SWAB STICKS is the device name listed in this FDA 510(k) record. The listed applicant is Acme United Corp.. It received FDA 510(k) clearance on 1983-10-31 under 510(k) number K833141. The device is classified under product code LKB. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ONE TIME ACETONE/ALCOHOL;SWAB STICKS?

ONE TIME ACETONE/ALCOHOL;SWAB STICKS is a medical device that received FDA 510(k) clearance on 1983-10-31. The listed applicant is Acme United Corp.. The 510(k) number is K833141.

When did ONE TIME ACETONE/ALCOHOL;SWAB STICKS receive FDA 510(k) clearance?

ONE TIME ACETONE/ALCOHOL;SWAB STICKS received FDA 510(k) clearance on 1983-10-31, under 510(k) number K833141.

Who is the listed applicant for ONE TIME ACETONE/ALCOHOL;SWAB STICKS?

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

What is the FDA product code for ONE TIME ACETONE/ALCOHOL;SWAB STICKS?

The FDA product code for ONE TIME ACETONE/ALCOHOL;SWAB STICKS is LKB.

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 Acme United 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 27 devices →

Related Devices (Code: LKB)

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.

↑