The following data is part of a premarket notification filed by Perimed, Inc. with the FDA for Peritemp Pf 4005 Heater.
Device ID | K932068 |
510k Number | K932068 |
Device Name: | PERITEMP PF 4005 HEATER |
Classification | Flowmeter, Blood, Cardiovascular |
Applicant | PERIMED, INC. 200 CENTENNIAL AVE. Piscataway, NJ 08854 -3910 |
Contact | Oystein Lind |
Correspondent | Oystein Lind PERIMED, INC. 200 CENTENNIAL AVE. Piscataway, NJ 08854 -3910 |
Product Code | DPW |
CFR Regulation Number | 870.2100 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-04-29 |
Decision Date | 1993-12-07 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
07332834000745 | K932068 | 000 |
07332834000516 | K932068 | 000 |
07332834000431 | K932068 | 000 |