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FDA 510(k)

BIONICARE STIMULATOR BIO-1

K-Number: K832805 · 1983-12-23

ApplicantMurray Electronics
Decision Date1983-12-23
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BIONICARE STIMULATOR BIO-1 is the device name listed in this FDA 510(k) record. The listed applicant is Murray Electronics. It received FDA 510(k) clearance on 1983-12-23 under 510(k) number K832805. 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 BIONICARE STIMULATOR BIO-1?

BIONICARE STIMULATOR BIO-1 is a medical device that received FDA 510(k) clearance on 1983-12-23. The listed applicant is Murray Electronics. The 510(k) number is K832805.

When did BIONICARE STIMULATOR BIO-1 receive FDA 510(k) clearance?

BIONICARE STIMULATOR BIO-1 received FDA 510(k) clearance on 1983-12-23, under 510(k) number K832805.

Who is the listed applicant for BIONICARE STIMULATOR BIO-1?

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

What is the FDA product code for BIONICARE STIMULATOR BIO-1?

The FDA product code for BIONICARE STIMULATOR BIO-1 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 Murray Electronics 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.

K983228BIONICARE STIMILATOR SYSTEM, MODEL BIO-1000K971437BIONICARE STIMULATOR SYSTEM. MODEL BIO-1000

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

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

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