The following data is part of a premarket notification filed by Cardiac Resucitator Corp. with the FDA for Stat-pad (tm).
Device ID | K871538 |
510k Number | K871538 |
Device Name: | STAT-PAD (TM) |
Classification | Pacemaker, Cardiac, External Transcutaneous (non-invasive) |
Applicant | CARDIAC RESUCITATOR CORP. 12244 S.W. GARDEN PLACE Portland, OR 97223 |
Contact | John L Karpowicz |
Correspondent | John L Karpowicz CARDIAC RESUCITATOR CORP. 12244 S.W. GARDEN PLACE Portland, OR 97223 |
Product Code | DRO |
CFR Regulation Number | 870.5550 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-04-20 |
Decision Date | 1987-06-24 |