The following data is part of a premarket notification filed by Stryker Corp. with the FDA for Stryker Powered Stretcher.
Device ID | K942948 |
510k Number | K942948 |
Device Name: | STRYKER POWERED STRETCHER |
Classification | Stretcher, Wheeled |
Applicant | STRYKER CORP. MEDICAL DIV. 6300 SPRINKLE RD. Kalamazoo, MI 49001 -6197 |
Contact | Richard Bartow |
Correspondent | Richard Bartow STRYKER CORP. MEDICAL DIV. 6300 SPRINKLE RD. Kalamazoo, MI 49001 -6197 |
Product Code | FPO |
CFR Regulation Number | 880.6910 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-06-23 |
Decision Date | 1995-01-24 |