Perkin-Elmer LC235 Diode Array Detector
FDA 510(k) K872737 · The Perkin-Elmer Corp.
510(k) numberK872737
Submission
- Device name
- Perkin-Elmer LC235 Diode Array Detector
- Applicant
- The Perkin-Elmer Corp.
- Received
- July 9, 1987
- Decision date
- September 18, 1987
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
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| K862605 | Modular Mass Spectrometer (M.S.)CCK · Traditional | 08/13/1986SE |
| K862178 | Isopure LC SystemLDM · Traditional | 07/14/1986SE |
Questions and answers
When was Perkin-Elmer LC235 Diode Array Detector cleared by the FDA?
Perkin-Elmer LC235 Diode Array Detector (K872737) received a 510(k) decision of Substantially Equivalent on September 18, 1987, 71 days after the submission was received.