Home / 510(k) Clearances / K872737

510(k) K872737

PERKIN-ELMER LC235 DIODE ARRAY DETECTOR by The Perkin-Elmer Corp.

K872737 is an FDA 510(k) premarket notification submitted by The Perkin-Elmer Corp. for the device "PERKIN-ELMER LC235 DIODE ARRAY DETECTOR". The FDA issued a decision of Substantially Equivalent on September 18, 1987. The Perkin-Elmer Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 18, 1987
Date Received
July 9, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by The Perkin-Elmer Corp.

  • K935666 — PERKIN-ELMER SERIES 200 LIQ CHROMATOGRAPHIC PUMP (April 26, 1994)
  • K900828 — PERKIN-ELMER AA 3100 ATOMIC ABSORPTION SPECTRO. (April 9, 1990)
  • K884864 — PLASMA 40 INDUCT. COUPLED PLASMA EMMISSION SPECTRO (February 10, 1989)
  • K884886 — MODEL 250 LIQUID CHROMOTAGRAPHY PUMP (February 2, 1989)
  • K872464 — ION TRAP DETECTOR (ITD) (August 11, 1987)
  • K871550 — PFI-20 POLARIZING FLUORIMETER (July 1, 1987)
  • K872122 — 8000 SERIES GAS CHROMATOGRAPHS (June 17, 1987)
  • K870661 — LIFEWATCH PLUS (March 9, 1987)
  • K862605 — MODULAR MASS SPECTROMETER (M.S.) (August 13, 1986)
  • K862178 — ISOPURE LC SYSTEM (July 14, 1986)

FDA data resources