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510(k) K850910

HUNTLEIGH FLOWTRON AIR, AC400/2 AIR by Huntleigh Technology, Inc.

K850910 is an FDA 510(k) premarket notification submitted by Huntleigh Technology, Inc. for the device "HUNTLEIGH FLOWTRON AIR, AC400/2 AIR". The FDA issued a decision of Substantially Equivalent on August 20, 1985. Huntleigh Technology, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 20, 1985
Date Received
March 5, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Huntleigh Technology, Inc.

  • K992733 — AKRON ATP9 TRACTION MACHINE (November 10, 1999)
  • K964699 — RHEO DOPPLEX II (RD 2) (February 21, 1997)
  • K924516 — OP3/VP4 (June 28, 1993)
  • K910188 — FLOWPLUS AC330 PUMP GARMENTS (May 28, 1991)
  • K900882 — MULTI DOPPLEX, MD-1 (August 22, 1990)
  • K900618 — HUNTLEIGH FETAL DOPPLER, FD-1 & DOPCORD, D140 (April 25, 1990)
  • K890012 — HUNTLEIGH DYNAMIC FLOTATION SYSTEM (March 29, 1989)
  • K884451 — DOPCORD PPG (January 12, 1989)
  • K881632 — FLOWTRON DVT SYSTEM AC500 PUMP, L501 GARMENT (September 26, 1988)
  • K874688 — FLOWTRON AC200/2 (September 23, 1988)

FDA data resources