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FDA 510(k)

SYNCHRO-LINK -CONTIN-PASSIVE MOTION DEVICE/MUSCLE

K-Number: K844995 · 1985-04-01

ApplicantCropper Medical, Inc.
Decision Date1985-04-01
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SYNCHRO-LINK -CONTIN-PASSIVE MOTION DEVICE/MUSCLE is the device name listed in this FDA 510(k) record. The listed applicant is Cropper Medical, Inc.. It received FDA 510(k) clearance on 1985-04-01 under 510(k) number K844995. 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 SYNCHRO-LINK -CONTIN-PASSIVE MOTION DEVICE/MUSCLE?

SYNCHRO-LINK -CONTIN-PASSIVE MOTION DEVICE/MUSCLE is a medical device that received FDA 510(k) clearance on 1985-04-01. The listed applicant is Cropper Medical, Inc.. The 510(k) number is K844995.

When did SYNCHRO-LINK -CONTIN-PASSIVE MOTION DEVICE/MUSCLE receive FDA 510(k) clearance?

SYNCHRO-LINK -CONTIN-PASSIVE MOTION DEVICE/MUSCLE received FDA 510(k) clearance on 1985-04-01, under 510(k) number K844995.

Who is the listed applicant for SYNCHRO-LINK -CONTIN-PASSIVE MOTION DEVICE/MUSCLE?

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

What is the FDA product code for SYNCHRO-LINK -CONTIN-PASSIVE MOTION DEVICE/MUSCLE?

The FDA product code for SYNCHRO-LINK -CONTIN-PASSIVE MOTION DEVICE/MUSCLE is BXB.

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 Cropper Medical, 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.

K871012CONTINUOUS PASSIVE MOTION PATIENT KIT OR RE. PAD

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.K955105BTE CPM-10Baltimore Therapeutic Equipment Co.K955106BTE CPM-20Baltimore Therapeutic Equipment Co.

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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