Submission Details
| 510(k) Number | K842752 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | July 16, 1984 |
| Decision Date | August 22, 1984 |
| Days to Decision | 37 days |
| Submission Type | Traditional |
| Review Panel | Toxicology (TX) |
| Summary | — |
K842752 is an FDA 510(k) clearance for the ZEEMAN 3030 ATOMIC ABSORPT SPECTORPHOT, 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 August 22, 1984, 37 days after receiving the submission on July 16, 1984. This device falls under the Toxicology review panel. Regulated under 21 CFR 862.2850.
| 510(k) Number | K842752 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | July 16, 1984 |
| Decision Date | August 22, 1984 |
| Days to Decision | 37 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 |