Submission Details
| 510(k) Number | K830799 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | March 14, 1983 |
| Decision Date | April 12, 1983 |
| Days to Decision | 29 days |
| Submission Type | Traditional |
| Review Panel | Toxicology (TX) |
| Summary | — |
K830799 is an FDA 510(k) clearance for the INDUCTIVELY-COUPLED PLASMA SPECTROMETER, a Atomic Absorption Spectrophotometer, General Use (Class I — General Controls, product code JXR), submitted by The Perkin-Elmer Corp. (Mchenry, US). The FDA issued a Cleared decision on April 12, 1983, 29 days after receiving the submission on March 14, 1983. This device falls under the Toxicology review panel. Regulated under 21 CFR 862.2850.
| 510(k) Number | K830799 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | March 14, 1983 |
| Decision Date | April 12, 1983 |
| Days to Decision | 29 days |
| Submission Type | Traditional |
| Review Panel | Toxicology (TX) |
| Summary | — |
| Product Code | JXR — Atomic Absorption Spectrophotometer, General Use |
| Device Class | Class I — General Controls |
| CFR Regulation | 21 CFR 862.2850 |