The following data is part of a premarket notification filed by Howell Ventures Ltd. with the FDA for Sure Grip, Hand Controls Model Sg-1.
| Device ID | K910072 |
| 510k Number | K910072 |
| Device Name: | SURE GRIP, HAND CONTROLS MODEL SG-1 |
| Classification | 510(k) Premarket Notification // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.S. Food & Drug Administration Follow FDA En Español Search FDA Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products 510(k) Premarket Notification Var MP = { Version: '1.0.22', Domains: {'es':'esp.fda.gov'}, SrcLang: 'en', UrlLang: 'mp_js_current_la |
| Applicant | HOWELL VENTURES LTD. RR #6 Fredericton, N.b., CA E3b 4x7 |
| Contact | Keith Howell |
| Correspondent | Keith Howell HOWELL VENTURES LTD. RR #6 Fredericton, N.b., CA E3b 4x7 |
| Product Code | IPQ |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-01-09 |
| Decision Date | 1991-01-23 |