The following data is part of a premarket notification filed by Intl. Immunoassay Laboratories, Inc. with the FDA for Isofor-mm (tm).
Device ID | K883222 |
510k Number | K883222 |
Device Name: | ISOFOR-MM (TM) |
Classification | U.v. Method, Cpk Isoenzymes |
Applicant | INTL. IMMUNOASSAY LABORATORIES, INC. 1900 WYATT DR., #11 Santa Clara, CA 95054 |
Contact | Shah, Ph.d. |
Correspondent | Shah, Ph.d. INTL. IMMUNOASSAY LABORATORIES, INC. 1900 WYATT DR., #11 Santa Clara, CA 95054 |
Product Code | JHW |
CFR Regulation Number | 862.1215 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-07-29 |
Decision Date | 1988-09-30 |