The following data is part of a premarket notification filed by Hyland Therapeutic Div., Travenol Laboratories with the FDA for Q-pak Chemistry Radioreceptor Control A.
Device ID | K770010 |
510k Number | K770010 |
Device Name: | Q-PAK CHEMISTRY RADIORECEPTOR CONTROL A |
Classification | Calibrator, Multi-analyte Mixture |
Applicant | HYLAND THERAPEUTIC DIV., TRAVENOL LABORATORIES 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | JIX |
CFR Regulation Number | 862.1150 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1977-01-03 |
Decision Date | 1977-04-18 |