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510(k) K833884

ISOTEC DISPOS. PRESSURE TRANSDUCER by Delta Medical Industries

K833884 is an FDA 510(k) premarket notification submitted by Delta Medical Industries for the device "ISOTEC DISPOS. PRESSURE TRANSDUCER". The FDA issued a decision of Substantially Equivalent on April 17, 1984. Delta Medical Industries has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 17, 1984
Date Received
November 9, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Delta Medical Industries

  • K840253 — ONE-WAY AIR VALVE (April 5, 1984)
  • K832470 — INFUSION PUMP (February 28, 1984)
  • K830389 — ACCU-RYNGE PUMP SP-250 (September 12, 1983)
  • K831750 — PM-3 (July 26, 1983)
  • K822761 — DELIVERY TUBE SET #2226 (September 30, 1982)
  • K820912 — PMS-2 PRESSURE MONITOR SEPARATOR (May 18, 1982)
  • K820482 — ACCU-RYNGE INSULIN PUMP #SP-250 (March 26, 1982)
  • K810068 — PEDIATRIC ARTERIAL BLOOD FILTER (January 22, 1981)
  • K802755 — ARTERIAL BLOOD FILTER BF-37 (January 7, 1981)
  • K803101 — PREBYPASS FILTER CAT.#K-5 (December 22, 1980)

FDA data resources