A Plus International, Inc. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
A Plus International, Inc. has 11 FDA 510(k) cleared general hospital devices. Based in La Puente, US.
Last cleared in 2022. Active since 1988.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Shanghai Sungo Management Consulting Company Limited. as regulatory consultant.
FDA 510(k) Regulatory Record - A Plus International, Inc.
11 devices
Cleared
May 11, 2022
Procedure Mask, Surgical Mask
General Hospital
233d
Cleared
Jan 13, 2011
SURGIPLUS SMS SURGICAL DRAPE (STERILE/NON-STERILE), SURGIPLUS SPP WITH PE...
General Hospital
105d
Cleared
Nov 12, 2009
SURGIPLUS STANDARD SURGICAL GOWN (STERILE) ( NON STERILE), REINFORCED...
General Hospital
36d
Cleared
Jun 19, 2003
SOLUTION FACE MASKS
General Hospital
51d
Cleared
Jun 23, 1988
COVER, SHOE OPERATING ROOM
General Hospital
23d
Cleared
Jun 23, 1988
GOWN, ISOLATION, SURGICAL (FYC)
General Hospital
23d
Cleared
Jun 23, 1988
SUIT, SURGICAL
General Hospital
23d
Cleared
Jun 23, 1988
BOUFFANT CAP
General & Plastic Surgery
23d
Cleared
Jun 23, 1988
SURGEONS CAP
General & Plastic Surgery
23d
Cleared
Apr 29, 1988
OPERATING ROOM TOWELS -STERILE & NON-STERILE
General Hospital
25d
Cleared
Apr 28, 1988
GAUZE AND LAP SPONGES -STERILE & NON-STERILE
General & Plastic Surgery
24d