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510(k) K841723

ADLER CUSTOM PROCEDURE PACKS by Adler Instrument Co.

K841723 is an FDA 510(k) premarket notification submitted by Adler Instrument Co. for the device "ADLER CUSTOM PROCEDURE PACKS". The FDA issued a decision of Substantially Equivalent on August 1, 1984. Adler Instrument Co. has at least 7 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 1, 1984
Date Received
April 25, 1984
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)
  • K833264 — ADLER STEAM INDICATOR-GAS INDICATOR (November 3, 1983)
  • K831068 — CONTAINER SYSTEM (May 9, 1983)

FDA data resources