The following data is part of a premarket notification filed by Physio-control Corp. with the FDA for Vsm R1.
Device ID | K842213 |
510k Number | K842213 |
Device Name: | VSM R1 |
Classification | Transducer, Pressure, Catheter Tip |
Applicant | PHYSIO-CONTROL CORP. 11811 WILLOWS RD. N.E. P.O. BOX 97006 Redmond, WA 98073 -9706 |
Contact | Michael B Gropp |
Correspondent | Michael B Gropp PHYSIO-CONTROL CORP. 11811 WILLOWS RD. N.E. P.O. BOX 97006 Redmond, WA 98073 -9706 |
Product Code | DXO |
CFR Regulation Number | 870.2870 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1984-06-04 |
Decision Date | 1984-10-26 |