Johnson & Johnson Clinical Diagnostics, Inc. · Class II · Cleared Jul 14, 1995
| K-number | K952211 |
| Device name | AMERLITE TSH-30 ULTRASENSITIVE ASSAY (LAN.0010Q/2010Q) |
| Applicant | Johnson & Johnson Clinical Diagnostics, Inc. |
| Product code | JLW |
| Device class | Class II |
| Decision date | Jul 14, 1995 |
| Decision | Substantially Equivalent |
| Regulation | 862.1690 |
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