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FDA 510(k)

STIMULATOR, FACIAL-MODELS SF-100 & 200

K-Number: K811502 · 1981-07-24

ApplicantRcx-Western, Inc.
Decision Date1981-07-24
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

STIMULATOR, FACIAL-MODELS SF-100 & 200 is the device name listed in this FDA 510(k) record. The listed applicant is Rcx-Western, Inc.. It received FDA 510(k) clearance on 1981-07-24 under 510(k) number K811502. 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 STIMULATOR, FACIAL-MODELS SF-100 & 200?

STIMULATOR, FACIAL-MODELS SF-100 & 200 is a medical device that received FDA 510(k) clearance on 1981-07-24. The listed applicant is Rcx-Western, Inc.. The 510(k) number is K811502.

When did STIMULATOR, FACIAL-MODELS SF-100 & 200 receive FDA 510(k) clearance?

STIMULATOR, FACIAL-MODELS SF-100 & 200 received FDA 510(k) clearance on 1981-07-24, under 510(k) number K811502.

Who is the listed applicant for STIMULATOR, FACIAL-MODELS SF-100 & 200?

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

What is the FDA product code for STIMULATOR, FACIAL-MODELS SF-100 & 200?

The FDA product code for STIMULATOR, FACIAL-MODELS SF-100 & 200 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 Rcx-Western, 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.

K811501EPILATOR, MULTIPLE NEEDLE-MODEL EM-20K811503EPILATOR, BLEND-MODEL EB-200 & ET-1

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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