FDA 510(k)

ULTRASONIC CLEANER

K-Number: K827508 · 1982-07-02

Decision Date1982-07-02

Product Code

DecisionSubstantially Equivalent

Device Summary

ULTRASONIC CLEANER is the device name listed in this FDA 510(k) record. The listed applicant is Keymed House. It received FDA 510(k) clearance on 1982-07-02 under 510(k) number K827508. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRASONIC CLEANER?

ULTRASONIC CLEANER is a medical device that received FDA 510(k) clearance on 1982-07-02. The listed applicant is Keymed House. The 510(k) number is K827508.

When did ULTRASONIC CLEANER receive FDA 510(k) clearance?

ULTRASONIC CLEANER received FDA 510(k) clearance on 1982-07-02, under 510(k) number K827508.

Who is the listed applicant for ULTRASONIC CLEANER?

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

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Keymed House as applicant

K827507ENDOSCOPIC ACCESSORY U/S/ CLEANING MACHINE

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.