The following data is part of a premarket notification filed by Bridgewater Mfg. Corp. with the FDA for Underpads, High Absorbant Polymer.
| Device ID | K781877 |
| 510k Number | K781877 |
| Device Name: | UNDERPADS, HIGH ABSORBANT POLYMER |
| Classification | Bandage, Liquid |
| Applicant | BRIDGEWATER MFG. CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KMF |
| CFR Regulation Number | 880.5090 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-11-06 |
| Decision Date | 1978-12-15 |