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510(k) K844092

DIAGNOSTIC MICROSOPCE SLIDES by Sybron Corp.

K844092 is an FDA 510(k) premarket notification submitted by Sybron Corp. for the device "DIAGNOSTIC MICROSOPCE SLIDES". The FDA issued a decision of Substantially Equivalent on October 25, 1984. Sybron Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 25, 1984
Date Received
October 19, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Sybron Corp.

  • K862284 — SEALITE (June 23, 1986)
  • K854855 — PROOF ALGINATE IMPRESSION MATERIAL (January 30, 1986)
  • K842132 — TYCOS SELF-CHECK/DIGITAL FEVER THERMO (July 18, 1984)
  • K841910 — KERR SEALAPEX ROOT CANAL SEALER (July 13, 1984)
  • K841732 — LIEBEL-FLARSHEIM AFC 1000 X-RAY FILM (June 5, 1984)
  • K840469 — TYCOS SELF CHECK BPM3 BLOOD PRESS MONI (May 21, 1984)
  • K840407 — KERR RESIN BONDED BRIDGE CEMENT (May 21, 1984)
  • K840607 — LF MOTORIZED RADIOGRAPHIC FILM VIEWER (March 5, 1984)
  • K833138 — DIGITAL INJECTOR SYS (November 14, 1983)
  • K823795 — EVERBOND GLASS IONOMER CEMENT (January 26, 1983)

FDA data resources