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FDA 510(k)

ACTION-WHEELS & PLAY WHEELS

K-Number: K850875 · 1985-05-16

ApplicantKetronic, Inc.
Decision Date1985-05-16
Product Code
DecisionSubstantially Equivalent

Device Summary

ACTION-WHEELS & PLAY WHEELS is the device name listed in this FDA 510(k) record. The listed applicant is Ketronic, Inc.. It received FDA 510(k) clearance on 1985-05-16 under 510(k) number K850875. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACTION-WHEELS & PLAY WHEELS?

ACTION-WHEELS & PLAY WHEELS is a medical device that received FDA 510(k) clearance on 1985-05-16. The listed applicant is Ketronic, Inc.. The 510(k) number is K850875.

When did ACTION-WHEELS & PLAY WHEELS receive FDA 510(k) clearance?

ACTION-WHEELS & PLAY WHEELS received FDA 510(k) clearance on 1985-05-16, under 510(k) number K850875.

Who is the listed applicant for ACTION-WHEELS & PLAY WHEELS?

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

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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.

K850877MONOLIFT MPE2, PLATFORM, CHAIR, FULLY FUTO PLATFORK850869MFE COUCH ERGOMETERK850873HILO TABLES, TYPE CH-4, CH-8, FW-6, FW-5, FW-2, ALK850870MEDIFETTE ERGOMETERK850868MFE CARDIAC STRESS SYSTEMK850872PHYACTION 300, 360, 370, 390 & 391 ELEC-MUSCLE-STI

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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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