FDA 510(k)

MINI PULSATOR

K-Number: K831474 · 1983-07-26

Decision Date1983-07-26

Product Code

DecisionSubstantially Equivalent

Device Summary

MINI PULSATOR is the device name listed in this FDA 510(k) record. The listed applicant is Medelco , Ltd.. It received FDA 510(k) clearance on 1983-07-26 under 510(k) number K831474. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINI PULSATOR?

MINI PULSATOR is a medical device that received FDA 510(k) clearance on 1983-07-26. The listed applicant is Medelco , Ltd.. The 510(k) number is K831474.

When did MINI PULSATOR receive FDA 510(k) clearance?

MINI PULSATOR received FDA 510(k) clearance on 1983-07-26, under 510(k) number K831474.

Who is the listed applicant for MINI PULSATOR?

The FDA 510(k) record lists Medelco , Ltd. 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 Medelco , Ltd. as applicant

K853767FLOSPIK K831472ULTRA PULSATOR K831473ULTRA PULSATOR MF

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.