The following data is part of a premarket notification filed by Klarity Medical Products, Llc with the FDA for Klarity Vacuum Bag, Klarity Mold Cushion.
| Device ID | K132124 |
| 510k Number | K132124 |
| Device Name: | KLARITY VACUUM BAG, KLARITY MOLD CUSHION |
| Classification | Accelerator, Linear, Medical |
| Applicant | KLARITY MEDICAL PRODUCTS, LLC 80 WESTGATE DRIVE Newark, OH 43055 |
| Contact | Peter Larson |
| Correspondent | Peter Larson KLARITY MEDICAL PRODUCTS, LLC 80 WESTGATE DRIVE Newark, OH 43055 |
| Product Code | IYE |
| CFR Regulation Number | 892.5050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-07-10 |
| Decision Date | 2013-11-01 |
| Summary: | summary |