C.L. Mcintosh & Assoc., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
C.L. Mcintosh & Assoc., Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
C.L. Mcintosh & Assoc., Inc. has 4 FDA 510(k) cleared medical devices. Based in Lexington, US.
Historical record: 4 cleared submissions from 1996 to 1997.
Browse the FDA 510(k) cleared devices submitted by C.L. Mcintosh & Assoc., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - C.L. Mcintosh & Assoc., Inc.
4 devices
Cleared
Dec 04, 1997
AUTIMO 2.5-D AND AUTIMO 3-D
Radiology
188d
Cleared
Jun 16, 1997
ORTHOSONICS DUO-SON ULTRASOUND DIATHERMY DEVICE
Physical Medicine
153d
Cleared
Aug 01, 1996
OSCAR ORTHOSONICS SYSTEM FOR CEMENTED ARTHROPLASTY REVISION
Orthopedic
90d
Cleared
Jun 28, 1996
NICAS 2001 NONINVASIVE CARDIO-RESPIRATORY SYSTEM
Cardiovascular
784d