Synchro-Link -Contin-Passive Motion Device/Muscle

FDA 510(k) K844995 · Cropper Medical, Inc.

Substantially Equivalent

510(k) numberK844995

Submission

Device name
Synchro-Link -Contin-Passive Motion Device/Muscle
Applicant
Cropper Medical, Inc.
Scottsdale, AZ, US
Received
December 26, 1984
Decision date
April 1, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
BXB – Exerciser, Powered
Device class
Class I (low risk)
Regulation
21 CFR 890.5380
Specialty
Physical Medicine

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More from Aquarius Electronics, Inc.

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K871012Continuous Passive Motion Patient Kit or Re. PadBXB · Traditional 03/25/1987SE

Questions and answers

When was Synchro-Link -Contin-Passive Motion Device/Muscle cleared by the FDA?

Synchro-Link -Contin-Passive Motion Device/Muscle (K844995) received a 510(k) decision of Substantially Equivalent on April 1, 1985, 96 days after the submission was received.

What is the product code of K844995?

The FDA product code is BXB – Exerciser, Powered, a Class I (low risk) device regulated under 21 CFR 890.5380.