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510(k) K954984

MINIBORE STOPCOCK SET by Distronic Sterile Products, Inc. — Product Code FMG

K954984 is an FDA 510(k) premarket notification submitted by Distronic Sterile Products, Inc. for the device "MINIBORE STOPCOCK SET". The FDA issued a decision of Substantially Equivalent on January 23, 1996. The device falls under product code FMG (Stopcock, I.V. Set), a Class II device regulated under 21 CFR 880.5440. Distronic Sterile Products, Inc. has at least 7 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 23, 1996
Date Received
October 31, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Stopcock, I.V. Set
Device Class
Class II
Regulation Number
880.5440
Review Panel
HO
Submission Type

Other clearances by Distronic Sterile Products, Inc.

  • K955709 — WINGED & SUBCUTANEOUS INFUSION SETS (February 21, 1996)
  • K955732 — VENTED SOLUTION SET (February 21, 1996)
  • K954983 — EXTENSION SET WITH CHECK VALVE (January 23, 1996)
  • K952664 — SOLUTION ADMINISTRATION SET (August 7, 1995)
  • K950597 — CORE-RESISTANT HUBER INFUSION SET WITH Y-SITE (July 26, 1995)
  • K952663 — 60 MICRO VOLUME EXTENSION SET W/.22 MICRON FILTER, 21 EXTENSION SET W/1.2 MIVTON (July 14, 1995)
  • K945184 — INTRAVASCULAR ADMINISTRATION SET (February 8, 1995)

Other clearances for product code FMG

  • K242255 — Qitexio® 4-Way Stopcock (QIT014) (April 29, 2025)
  • K223499 — Three Way Stop Cock (July 21, 2023)
  • K223175 — lntravascular Administration Sets with Stopcock and Manifold (March 10, 2023)
  • K211204 — SafePort(TM) Manifold (or Stopcock) (September 15, 2022)
  • K210516 — Clicky Cross (May 16, 2022)
  • K190539 — TurnSignal Stopcocks Sterile, TurnSignal Stopcocks Buld Non Sterile, TurnSignal (October 22, 2019)
  • K190489 — Elcam Stopcocks and Manifolds (April 23, 2019)
  • K172266 — Dynarex Three-Way Stopcock (March 14, 2018)
  • K141254 — ELCAM STOPCOCKS AND MANIFOLDS (July 30, 2014)
  • K123084 — DISPOSABLE HIGH PRESSURE STOPCOCK/MANIFOLD MODEL HP STOPCOCK, MP STOPCOCK, HP MA (May 23, 2013)

FDA data resources