The following data is part of a premarket notification filed by Mallinckrodt Critical Care with the FDA for Diagnostic Intravascular Catheters.
Device ID | K853182 |
510k Number | K853182 |
Device Name: | DIAGNOSTIC INTRAVASCULAR CATHETERS |
Classification | Catheter, Intravascular, Diagnostic |
Applicant | MALLINCKRODT CRITICAL CARE 675 MCDONNELL BLVD. P.O. BOX 5840 St Louis, MO 63134 |
Contact | Carol L Mcnail-sabo |
Correspondent | Carol L Mcnail-sabo MALLINCKRODT CRITICAL CARE 675 MCDONNELL BLVD. P.O. BOX 5840 St Louis, MO 63134 |
Product Code | DQO |
CFR Regulation Number | 870.1200 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-07-30 |
Decision Date | 1986-01-15 |