The following data is part of a premarket notification filed by Atomic Products Corp. with the FDA for Mri Stretcher.
Device ID | K874332 |
510k Number | K874332 |
Device Name: | MRI STRETCHER |
Classification | Stretcher, Wheeled |
Applicant | ATOMIC PRODUCTS CORP. P.O. DRAWER R Shirley, NY 11967 |
Contact | James Reiss |
Correspondent | James Reiss ATOMIC PRODUCTS CORP. P.O. DRAWER R Shirley, NY 11967 |
Product Code | FPO |
CFR Regulation Number | 880.6910 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-10-22 |
Decision Date | 1988-01-05 |