Medical Device Manufacturer · US , Wyckoff , NJ

Wfr/Aquaplast Corp. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1994

8

Total

8

Cleared

0

Denied

Wfr/Aquaplast Corp. has 8 FDA 510(k) cleared medical devices. Based in Wyckoff, US.

Historical record: 8 cleared submissions from 1994 to 2012. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Wfr/Aquaplast Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Wfr/Aquaplast Corp.

8 devices

1-8 of 8

Cleared Jun 20, 2012

QFIX RADIOTHERAPY CHAIR

Radiology · 85d

Cleared May 04, 2006

KVUE IGRT TREATMENT TABLE TOP, RT-4551KV, KVUE INSERTS AND ACCESSORIES, VARIOUS

Radiology · 51d

Cleared Sep 02, 2003

ACCUFIX RADIOLUCENT PELVIS AND BELLY BOARDS, ACCUFIX CANTILEVER HEAD BOARD...

Radiology · 50d

Cleared Jul 02, 2002

ACCUFIX TILTING RADIOTRANSLUCENT HEADHOLDER

Radiology · 85d

Cleared Dec 02, 1997

AQUAPLAST PALATAL STENT

Cleared Sep 30, 1994

AQUAPLAST TIE DOWN DRESSING

General & Plastic Surgery · 53d

Cleared Jul 29, 1994

AQUAPLAST NASAL SPLINTS, PRECUT SILVER SPLINT PATTERNS AND SPLINT KITS

Ear, Nose, Throat · 87d

Cleared May 26, 1994

Radiology · 218d