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510(k) K832626

TOP STERILE DISPOS. HYPODERMIC NEEDLES by Top Surgical Manufacturers Co. — Product Code GAA

K832626 is an FDA 510(k) premarket notification submitted by Top Surgical Manufacturers Co. for the device "TOP STERILE DISPOS. HYPODERMIC NEEDLES". The FDA issued a decision of Substantially Equivalent on October 14, 1983. The device falls under product code GAA (Needle, Aspiration And Injection, Disposable), a Class I device regulated under 21 CFR 878.4800. Top Surgical Manufacturers Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 14, 1983
Date Received
August 4, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Needle, Aspiration And Injection, Disposable
Device Class
Class I
Regulation Number
878.4800
Review Panel
SU
Submission Type

Other clearances by Top Surgical Manufacturers Co.

  • K844343 — TOP SINGLE USE U.T.W. A-V FISTULA NEEDLE Y TYPE (January 8, 1985)
  • K843415 — TOP HYPODERMIC SYRINGE LUER LOCK (December 7, 1984)
  • K843313 — TOP DISPOSABLE SPINAL NEEDLE (September 19, 1984)
  • K843414 — TOP HYPODERMIC SYRINGE PISTON (September 7, 1984)
  • K841119 — TOPS DISPOS. INFUSION SET/HEMODIALYSIS (April 20, 1984)
  • K841025 — TOP DISPOSABLE INFUSION SET (March 30, 1984)
  • K832624 — TOP VENULA I.V. CATHETER SET (November 21, 1983)
  • K832625 — TOP THREE WAY STOPCOCK (October 19, 1983)
  • K832622 — WINGED INFUSION SET (October 14, 1983)
  • K832621 — TOP DISPOSABLE PLASTIC SYRINGES (October 14, 1983)

Other clearances for product code GAA

  • K223625 — CapnoSpot™ Pneumothorax Decompression Indicator (March 28, 2023)
  • K102274 — ARVIK LAPAROSCOPIC ASPIRATION INSTRUMENT (June 15, 2011)
  • K011586 — IRMA SL BLOOD ANALYSIS SYSTEM GL CARTRIDGE (November 16, 2001)
  • K994151 — PERCUTX-INJECTION/ASPIRATION NEEDLE PROBES/DEVICES (March 1, 2000)
  • K983200 — INJECTION/ASPIRATION NEEDLES PROBES/DEVICES-TPI/TPI FLEX (December 11, 1998)
  • K974741 — MANAN ACCURA NEEDLE (January 8, 1998)
  • K962425 — BONOPTY COAXIAL BONE BIOPSY SYSTEM WITH ECCENTRIC DRILL(10-1072,3,4) (September 11, 1996)
  • K961959 — MD TECH BIOPSY SET FOR BONE AND BONE MARROW (July 19, 1996)
  • K945109 — MONOJECT BONE MARROW BIOPSY TRAYS (November 14, 1994)
  • K940024 — MANAN GENERAL PURPOSE INTRODUCER NEEDLE (February 25, 1994)

FDA data resources