The following data is part of a premarket notification filed by W. Murphy Ent., Inc. with the FDA for Weevac 6 Infant Evacuation Stretcher.
| Device ID | K902521 |
| 510k Number | K902521 |
| Device Name: | WEEVAC 6 INFANT EVACUATION STRETCHER |
| Classification | Stretcher, Hand-carried |
| Applicant | W. MURPHY ENT., INC. 48 SOUTHVALE DRIVE, TORONTO Ontario, CA M4g 1g3 |
| Contact | Murphy R.t. |
| Correspondent | Murphy R.t. W. MURPHY ENT., INC. 48 SOUTHVALE DRIVE, TORONTO Ontario, CA M4g 1g3 |
| Product Code | FPP |
| CFR Regulation Number | 880.6900 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-06-07 |
| Decision Date | 1990-06-22 |