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)

UCS-2, ULTRASONIC CLEANING SOLUTION

K-Number: K861147 · 1986-06-23

ApplicantKeymed, Inc.
Decision Date1986-06-23
Product CodeFLG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

UCS-2, ULTRASONIC CLEANING SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Keymed, Inc.. It received FDA 510(k) clearance on 1986-06-23 under 510(k) number K861147. The device is classified under product code FLG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UCS-2, ULTRASONIC CLEANING SOLUTION?

UCS-2, ULTRASONIC CLEANING SOLUTION is a medical device that received FDA 510(k) clearance on 1986-06-23. The listed applicant is Keymed, Inc.. The 510(k) number is K861147.

When did UCS-2, ULTRASONIC CLEANING SOLUTION receive FDA 510(k) clearance?

UCS-2, ULTRASONIC CLEANING SOLUTION received FDA 510(k) clearance on 1986-06-23, under 510(k) number K861147.

Who is the listed applicant for UCS-2, ULTRASONIC CLEANING SOLUTION?

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

What is the FDA product code for UCS-2, ULTRASONIC CLEANING SOLUTION?

The FDA product code for UCS-2, ULTRASONIC CLEANING SOLUTION is FLG.

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 Keymed, 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 29 devices →

Related Devices (Code: FLG)

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.

↑