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510(k) K831068

CONTAINER SYSTEM by Adler Instrument Co.

K831068 is an FDA 510(k) premarket notification submitted by Adler Instrument Co. for the device "CONTAINER SYSTEM". The FDA issued a decision of Substantially Equivalent on May 9, 1983. Adler Instrument Co. has at least 7 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 9, 1983
Date Received
April 4, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Adler Instrument Co.

  • K910170 — MAXI-FLOW SUCTION SET 12 FT. (February 1, 1991)
  • K910171 — MAXI-FLOW SUCTION SET W/Y CONNECTOR (February 1, 1991)
  • K903209 — MAXI-FLOW INSUFFLATOR TUBING SET W/FILTER (December 21, 1990)
  • K903208 — MAXI-FLOW INSUFFLATOR TUBING SET (December 17, 1990)
  • K900913 — ADLER DISPOSABLE BIPOLAR CORD (April 4, 1990)
  • K841723 — ADLER CUSTOM PROCEDURE PACKS (August 1, 1984)
  • K833264 — ADLER STEAM INDICATOR-GAS INDICATOR (November 3, 1983)

FDA data resources