The following data is part of a premarket notification filed by Hobbs Medical, Inc. with the FDA for Hobbs Medical Retrieval Basket.
| Device ID | K833124 |
| 510k Number | K833124 |
| Device Name: | HOBBS MEDICAL RETRIEVAL BASKET |
| Classification | Endoscopic Grasping/cutting Instrument, Non-powered |
| Applicant | HOBBS MEDICAL, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | OCZ |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-09-13 |
| Decision Date | 1983-11-29 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| M84948500 | K833124 | 000 |
| M84948320 | K833124 | 000 |
| M84948300 | K833124 | 000 |
| M84948240 | K833124 | 000 |
| M84948220 | K833124 | 000 |
| M84948160 | K833124 | 000 |
| M84948140 | K833124 | 000 |
| M84948080 | K833124 | 000 |
| M84948060 | K833124 | 000 |