The following data is part of a premarket notification filed by Angiodynamics, Inc. with the FDA for Angiodynamic, Inc. Morpheus Ct Picc And Procedure Kit.
Device ID | K060887 |
510k Number | K060887 |
Device Name: | ANGIODYNAMIC, INC. MORPHEUS CT PICC AND PROCEDURE KIT |
Classification | Catheter, Intravascular, Therapeutic, Long-term Greater Than 30 Days |
Applicant | ANGIODYNAMICS, INC. 603 QUEENSBURY AVE. Queensbury, NY 12804 |
Contact | Teri Juckett |
Correspondent | Teri Juckett ANGIODYNAMICS, INC. 603 QUEENSBURY AVE. Queensbury, NY 12804 |
Product Code | LJS |
CFR Regulation Number | 880.5970 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-03-31 |
Decision Date | 2006-04-28 |