The following data is part of a premarket notification filed by Miles, Inc. with the FDA for Ck-mb Method For The Technicon Immuno 1(r) System In-vitro Diagnostic System.
Device ID | K950186 |
510k Number | K950186 |
Device Name: | CK-MB METHOD FOR THE TECHNICON IMMUNO 1(R) SYSTEM IN-VITRO DIAGNOSTIC SYSTEM |
Classification | U.v. Method, Cpk Isoenzymes |
Applicant | MILES, INC. 511 BENEDICT AVE. Tarrytown, NY 10591 -5097 |
Contact | Gabriel J Muraca, Jr. |
Correspondent | Gabriel J Muraca, Jr. MILES, INC. 511 BENEDICT AVE. Tarrytown, NY 10591 -5097 |
Product Code | JHW |
CFR Regulation Number | 862.1215 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-01-17 |
Decision Date | 1995-03-13 |