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510(k) K925691

INSUFFLATION TUBING by Mectra Labs, Inc. — Product Code HIF

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 23, 1993
Date Received
November 12, 1992
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 Mectra Labs, Inc.

  • K113080 — TUBALGATOR (June 29, 2012)
  • K033880 — ELECTRO-LUBE (March 10, 2004)
  • K021247 — PNEUMOPERITONEUM INSUFFLATION NEEDLE (November 8, 2002)
  • K993604 — ENDOSCOPIC ANTI FOG DEVICE (March 3, 2000)
  • K955352 — SUCTION CAUTERY PROBE (April 5, 1996)
  • K934547 — MECTRA TROCAR (February 18, 1994)
  • K935382 — GRASPERS (February 15, 1994)
  • K920959 — INSUFFLATOR, LAPAROSCOPIC (July 13, 1992)

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)