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FDA 510(k)

MONOLIFT MPE2, PLATFORM, CHAIR, FULLY FUTO PLATFOR

K-Number: K850877 · 1985-06-12

ApplicantKetronic, Inc.
Decision Date1985-06-12
Product CodeILK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MONOLIFT MPE2, PLATFORM, CHAIR, FULLY FUTO PLATFOR is the device name listed in this FDA 510(k) record. The listed applicant is Ketronic, Inc.. It received FDA 510(k) clearance on 1985-06-12 under 510(k) number K850877. The device is classified under product code ILK. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MONOLIFT MPE2, PLATFORM, CHAIR, FULLY FUTO PLATFOR?

MONOLIFT MPE2, PLATFORM, CHAIR, FULLY FUTO PLATFOR is a medical device that received FDA 510(k) clearance on 1985-06-12. The listed applicant is Ketronic, Inc.. The 510(k) number is K850877.

When did MONOLIFT MPE2, PLATFORM, CHAIR, FULLY FUTO PLATFOR receive FDA 510(k) clearance?

MONOLIFT MPE2, PLATFORM, CHAIR, FULLY FUTO PLATFOR received FDA 510(k) clearance on 1985-06-12, under 510(k) number K850877.

Who is the listed applicant for MONOLIFT MPE2, PLATFORM, CHAIR, FULLY FUTO PLATFOR?

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

What is the FDA product code for MONOLIFT MPE2, PLATFORM, CHAIR, FULLY FUTO PLATFOR?

The FDA product code for MONOLIFT MPE2, PLATFORM, CHAIR, FULLY FUTO PLATFOR is ILK.

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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, ALK850870MEDIFETTE ERGOMETERK850868MFE CARDIAC STRESS SYSTEMK850872PHYACTION 300, 360, 370, 390 & 391 ELEC-MUSCLE-STIK850871TREDBAND TYPE I, IT, II & III - TREADMILLS

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Related Devices (Code: ILK)

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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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