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FDA 510(k)

IF-II (TM), MODEL 7200

K-Number: K923914 · 1992-11-06

ApplicantMedical Devices, Inc.
Decision Date1992-11-06
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

IF-II (TM), MODEL 7200 is the device name listed in this FDA 510(k) record. The listed applicant is Medical Devices, Inc.. It received FDA 510(k) clearance on 1992-11-06 under 510(k) number K923914. 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 IF-II (TM), MODEL 7200?

IF-II (TM), MODEL 7200 is a medical device that received FDA 510(k) clearance on 1992-11-06. The listed applicant is Medical Devices, Inc.. The 510(k) number is K923914.

When did IF-II (TM), MODEL 7200 receive FDA 510(k) clearance?

IF-II (TM), MODEL 7200 received FDA 510(k) clearance on 1992-11-06, under 510(k) number K923914.

Who is the listed applicant for IF-II (TM), MODEL 7200?

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

What is the FDA product code for IF-II (TM), MODEL 7200?

The FDA product code for IF-II (TM), MODEL 7200 is IPF.

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Other records listing Medical Devices, 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.

K002280PAD PRO PEDIATRIC ELECTRODE, MODEL PAD PRO 2602K930084MICRO-ARTHROSCOPEK943126ELECTROFLEXK940012SMARTBRACE ELECTRODEK935132HOME MICROCURRENT HMCK934619FLEXMATE

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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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