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 |