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FDA 510(k)

VACUPULSE VACUUM UNIT

K-Number: K842268 · 1984-07-20

ApplicantI-Rep, Inc.
Decision Date1984-07-20
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

VACUPULSE VACUUM UNIT is the device name listed in this FDA 510(k) record. The listed applicant is I-Rep, Inc.. It received FDA 510(k) clearance on 1984-07-20 under 510(k) number K842268. 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 VACUPULSE VACUUM UNIT?

VACUPULSE VACUUM UNIT is a medical device that received FDA 510(k) clearance on 1984-07-20. The listed applicant is I-Rep, Inc.. The 510(k) number is K842268.

When did VACUPULSE VACUUM UNIT receive FDA 510(k) clearance?

VACUPULSE VACUUM UNIT received FDA 510(k) clearance on 1984-07-20, under 510(k) number K842268.

Who is the listed applicant for VACUPULSE VACUUM UNIT?

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

What is the FDA product code for VACUPULSE VACUUM UNIT?

The FDA product code for VACUPULSE VACUUM UNIT is IPF.

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Other records listing I-Rep, 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.

K930692LATHAM TABLEK930691ACCUTRAC TRACTION UNITK861864MEDTRON TYPE P-300 ULTRASONIC THERAPY UNITK854947REHABILITATION TABLESK851690ADJUSTABLE TREATMENT TABLESK832940ROTAGYM

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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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