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FDA 510(k)

TREDBAND TYPE I, IT, II & III - TREADMILLS

K-Number: K850871 · 1985-06-05

ApplicantKetronic, Inc.
Decision Date1985-06-05
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TREDBAND TYPE I, IT, II & III - TREADMILLS is the device name listed in this FDA 510(k) record. The listed applicant is Ketronic, Inc.. It received FDA 510(k) clearance on 1985-06-05 under 510(k) number K850871. The device is classified under product code BXB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TREDBAND TYPE I, IT, II & III - TREADMILLS?

TREDBAND TYPE I, IT, II & III - TREADMILLS is a medical device that received FDA 510(k) clearance on 1985-06-05. The listed applicant is Ketronic, Inc.. The 510(k) number is K850871.

When did TREDBAND TYPE I, IT, II & III - TREADMILLS receive FDA 510(k) clearance?

TREDBAND TYPE I, IT, II & III - TREADMILLS received FDA 510(k) clearance on 1985-06-05, under 510(k) number K850871.

Who is the listed applicant for TREDBAND TYPE I, IT, II & III - TREADMILLS?

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 TREDBAND TYPE I, IT, II & III - TREADMILLS?

The FDA product code for TREDBAND TYPE I, IT, II & III - TREADMILLS is BXB.

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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 SYSTEMK850872PHYACTION 300, 360, 370, 390 & 391 ELEC-MUSCLE-STI

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Related Devices (Code: BXB)

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.

K072887G-TRAINER MEDICALAlter-G, Inc.K003272FLO-BOOTDiscovery Group, LLCK952975ANKLE CALF EXERCISER PHLEBOPUMPPrevent Products, Inc.K953456E-Z FLEXFluid Motion Biotechnologies, Inc.K955106BTE CPM-20Baltimore Therapeutic Equipment Co.K955105BTE CPM-10Baltimore Therapeutic Equipment Co.

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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