Home / 510(k) Clearances / K936155

510(k) K936155

ADAIR INSUFFLATION AND INSTRUMENTATION CANNULA by Micromedical Devices, Inc. — Product Code HIF

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 11, 1994
Date Received
December 27, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Insufflator, Laparoscopic
Device Class
Class II
Regulation Number
884.1730
Review Panel
OB
Submission Type

Other clearances by Micromedical Devices, Inc.

  • K043287 — PALMSCAN AP2000; PALMSCAN A2000; PALMSCAN P2000 (December 10, 2004)
  • K936195 — LAPAROSCOPES (August 17, 1994)
  • K936097 — VIDEO CAMERAS, ENCOSCOPIC AND SURGICAL (March 31, 1994)
  • K936086 — STERILE VIDEO CAMERA COVER AND DRAPE (March 17, 1994)
  • K850791 — MDI 2000 - PULSE GENERATOR (June 19, 1985)
  • K834262 — TRANS-PACE (February 4, 1984)

Other clearances for product code HIF

  • K250388 — ENDOFLATOR + (September 22, 2025)
  • K242772 — AirSurgN Insufflator (10030/AirSurgN) (April 11, 2025)
  • K243527 — High Flow Insufflation Unit (UHI-4) (January 13, 2025)
  • K242536 — TauTona Pneumoperitoneum Assist Device (TPAD) (October 15, 2024)
  • K232464 — VereSee Optical Veres Needle System (May 2, 2024)
  • K232902 — EVA15 insufflator (May 2, 2024)
  • K233020 — TauTona Pneumoperitoneum Assist Device (TPAD) (January 12, 2024)
  • K232401 — Disposable Veress Needles (December 14, 2023)
  • K231342 — Insufflator (OPTO-IFL1000) (September 20, 2023)
  • K230239 — AirSeal iFS System; AirSeal dV Solution (September 20, 2023)