The following data is part of a premarket notification filed by Transidyne General Corp. with the FDA for Bodily Fluid Disposal Kit.
| Device ID | K961217 |
| 510k Number | K961217 |
| Device Name: | BODILY FLUID DISPOSAL KIT |
| Classification | Mask, Surgical |
| Applicant | TRANSIDYNE GENERAL CORP. 400 HERALD JOURNAL PARK Spartanburg, SC 29303 |
| Contact | Steven W Butler |
| Correspondent | Steven W Butler TRANSIDYNE GENERAL CORP. 400 HERALD JOURNAL PARK Spartanburg, SC 29303 |
| Product Code | FXX |
| CFR Regulation Number | 878.4040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-03-28 |
| Decision Date | 1996-07-25 |