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FDA 510(k)

ULTRA PULSATOR MF

K-Number: K831473 · 1983-07-26

ApplicantMedelco , Ltd.
Decision Date1983-07-26
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ULTRA PULSATOR MF 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 K831473. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRA PULSATOR MF?

ULTRA PULSATOR MF 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 K831473.

When did ULTRA PULSATOR MF receive FDA 510(k) clearance?

ULTRA PULSATOR MF received FDA 510(k) clearance on 1983-07-26, under 510(k) number K831473.

Who is the listed applicant for ULTRA PULSATOR MF?

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

What is the FDA product code for ULTRA PULSATOR MF?

The FDA product code for ULTRA PULSATOR MF is IPF.

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.

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Other records listing Medelco , Ltd. 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.

K853767FLOSPIKK831472ULTRA PULSATORK831474MINI PULSATOR

Related Devices (Code: IPF)

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.

K253542Apollo Quattro (APQ-10M)Weero Co., Ltd.K252816High Tone Power therapy (HiToP) (Model: HiToP PNP)Mohammadali NezakatiK260142StimelMD (SSMD) systemMotion Informatics ltd.K251083Compact IIEnraf-Nonius, B.V.K241433EVE Synergy (EVE-20M)Weero Co., Ltd.K241488TrainFES AdvanceTrainfes

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.

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