The following data is part of a premarket notification filed by 3m Health Care, Ltd. with the FDA for 3m Model 200rt Rate Taper Infusion Pump.
Device ID | K926059 |
510k Number | K926059 |
Device Name: | 3M MODEL 200RT RATE TAPER INFUSION PUMP |
Classification | Scale, Patient |
Applicant | 3M HEALTH CARE, LTD. 3M CENTER, BLDG. 275-3E-08 P.O. BOX 33275 St. Paul, MN 55133 |
Contact | Von Busch |
Correspondent | Von Busch 3M HEALTH CARE, LTD. 3M CENTER, BLDG. 275-3E-08 P.O. BOX 33275 St. Paul, MN 55133 |
Product Code | FRW |
CFR Regulation Number | 880.2720 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-12-01 |
Decision Date | 1993-08-16 |