The following data is part of a premarket notification filed by Nipro Medical Corporation with the FDA for Nipro Safetouch Psv Scalp Vein Set With Safety Device.
Device ID | K140136 |
510k Number | K140136 |
Device Name: | NIPRO SAFETOUCH PSV SCALP VEIN SET WITH SAFETY DEVICE |
Classification | Catheter, Intravascular, Therapeutic, Short-term Less Than 30 Days |
Applicant | NIPRO MEDICAL CORPORATION 3150 N.W. 107TH AVE. Doral, FL 33172 |
Contact | Jessica Oswald-mcleod |
Correspondent | Jessica Oswald-mcleod NIPRO MEDICAL CORPORATION 3150 N.W. 107TH AVE. Doral, FL 33172 |
Product Code | FOZ |
CFR Regulation Number | 880.5200 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-01-17 |
Decision Date | 2014-02-14 |
Summary: | summary |