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510(k) K901744

DOBBHOFF(R) RETRIEVAL FORCEPS by Biosearch Medical Products, Inc. — Product Code KQW

K901744 is an FDA 510(k) premarket notification submitted by Biosearch Medical Products, Inc. for the device "DOBBHOFF(R) RETRIEVAL FORCEPS". The FDA issued a decision of Substantially Equivalent on July 3, 1990. The device falls under product code KQW (Goniometer, Nonpowered), a Class I device regulated under 21 CFR 888.1520. Biosearch Medical Products, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 3, 1990
Date Received
April 17, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Goniometer, Nonpowered
Device Class
Class I
Regulation Number
888.1520
Review Panel
NE
Submission Type

Other clearances by Biosearch Medical Products, Inc.

  • K051480 — ENTERAL FEEDING TUBE (October 12, 2005)
  • K970145 — PERINEOMETER & VAGINAL PROBE (BIOFEEDBACK MONITOR #20 AND VAGINAL PROBE) (August 11, 1997)
  • K964871 — BIOSEARCH SYRING FLUSHING/CLEANING PUMP FOR BIOSEARCH ENDOSCOPIC INSTRUMENTS (March 3, 1997)
  • K951260 — URINARY INTERMITTENT CATHETERS W/O HYDROMER HYDROPHILIC LUBRICANT (September 27, 1995)
  • K944614 — MEGA-BRUSH, ENDOSCOPIC MASS CYTOLOGY - CELLUAR RETRIEVAL SYSTEM (April 5, 1995)
  • K932295 — NON-BALLOON REPLACEMENT GASTROSTOMY KIT (September 8, 1994)
  • K935045 — BIOSEARCH LAPROSCOPIC GASTRONOMY CATHETER (August 19, 1994)
  • K923002 — ENTEROCLYSIS TUBE (June 28, 1994)
  • K934193 — CELL-MATE(TM) MASS CYTOLOGY-CELLULAR RETRIEVAL SYST (November 19, 1993)
  • K922987 — LAPSTICK LAPAROSCOPIC SPONGE STICK/ BLUNT DISSEC. (April 23, 1993)

Other clearances for product code KQW

  • K926237 — O'BRIEN GONIOMETER (August 2, 1993)
  • K870767 — THE (CROM) TESTER (March 17, 1987)
  • K850082 — HAND HELD GONIOMETER (April 4, 1985)
  • K831550 — FINGER BONIOMETER BK7506 (June 24, 1983)
  • K812778 — THE TELOS EQUIPMENT (December 8, 1981)
  • K810441 — UNIVERSAL GONIMETER (February 27, 1981)
  • K801717 — BK-7511 BRASS GONIOMETER (August 4, 1980)
  • K801716 — BK-7505 RADIOPAQUE GONIOMETER, 8 (August 4, 1980)
  • K801718 — BK-7513 STAINLESS STEEL GONIOMETER (August 4, 1980)
  • K801715 — BK-7497 BULB DYNAMOMETER (August 4, 1980)

FDA data resources