The following data is part of a premarket notification filed by Skil-care Corp. with the FDA for Support Vest.
Device ID | K963459 |
510k Number | K963459 |
Device Name: | SUPPORT VEST |
Classification | Restraint, Wheelchair, Non-protective |
Applicant | SKIL-CARE CORP. 167 SAW MILL RIVER RD. Yonkers, NY 10701 |
Contact | Arnold Silverman |
Correspondent | Arnold Silverman SKIL-CARE CORP. 167 SAW MILL RIVER RD. Yonkers, NY 10701 |
Product Code | KID |
CFR Regulation Number | 890.3910 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-09-03 |
Decision Date | 1996-10-15 |
Summary: | summary |