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FDA 510(k)

PHYACTION 300, 360, 370, 390 & 391 ELEC-MUSCLE-STI

K-Number: K850872 · 1985-06-06

ApplicantKetronic, Inc.
Decision Date1985-06-06
Product Code
DecisionSubstantially Equivalent for Some Indications

Device Summary

PHYACTION 300, 360, 370, 390 & 391 ELEC-MUSCLE-STI is the device name listed in this FDA 510(k) record. The listed applicant is Ketronic, Inc.. It received FDA 510(k) clearance on 1985-06-06 under 510(k) number K850872. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the PHYACTION 300, 360, 370, 390 & 391 ELEC-MUSCLE-STI?

PHYACTION 300, 360, 370, 390 & 391 ELEC-MUSCLE-STI is a medical device that received FDA 510(k) clearance on 1985-06-06. The listed applicant is Ketronic, Inc.. The 510(k) number is K850872.

When did PHYACTION 300, 360, 370, 390 & 391 ELEC-MUSCLE-STI receive FDA 510(k) clearance?

PHYACTION 300, 360, 370, 390 & 391 ELEC-MUSCLE-STI received FDA 510(k) clearance on 1985-06-06, under 510(k) number K850872.

Who is the listed applicant for PHYACTION 300, 360, 370, 390 & 391 ELEC-MUSCLE-STI?

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

Related Clinical Trials

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Other records listing Ketronic, 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.

K850869MFE COUCH ERGOMETERK850873HILO TABLES, TYPE CH-4, CH-8, FW-6, FW-5, FW-2, ALK850877MONOLIFT MPE2, PLATFORM, CHAIR, FULLY FUTO PLATFORK850870MEDIFETTE ERGOMETERK850868MFE CARDIAC STRESS SYSTEMK850871TREDBAND TYPE I, IT, II & III - TREADMILLS

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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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