Penner Manufacturing, Inc. is one of 24892 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Penner Manufacturing, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PACIFIC RECUMBENT HEIGHT-ADJUSTABLE BATH SYSTEM, CASCADE BATH, MODEL 6900, SUPERIOR BATH, MODEL 6300
3
Total
3
Cleared
0
Denied
Penner Manufacturing, Inc. has 3 FDA 510(k) cleared medical devices. Based in Ohaha, US.
Historical record: 3 cleared submissions from 2001 to 2004. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Penner Manufacturing, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Penner Manufacturing, Inc.
3 devices