Perkin-Elmer LC235 Diode Array Detector

FDA 510(k) K872737 · The Perkin-Elmer Corp.

Substantially Equivalent

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)

Official FDA 510(k) record

Device classification

No product code recorded.

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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.