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510(k) K760264

CURETTE, PROPOSED TIS-U-TRAP, METAL by Milex Products, Inc. — Product Code HHK

K760264 is an FDA 510(k) premarket notification submitted by Milex Products, Inc. for the device "CURETTE, PROPOSED TIS-U-TRAP, METAL". The FDA issued a decision of Substantially Equivalent on October 6, 1976. The device falls under product code HHK (Curette, Suction, Endometrial (And Accessories)), a Class II device regulated under 21 CFR 884.1175. Milex Products, Inc. has at least 7 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 6, 1976
Date Received
July 21, 1976
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Curette, Suction, Endometrial (And Accessories)
Device Class
Class II
Regulation Number
884.1175
Review Panel
OB
Submission Type

Other clearances by Milex Products, Inc.

  • K001545 — PIPET CURET (June 15, 2000)
  • K904774 — INGLAT-O-BALL (December 7, 1990)
  • K904026 — INFLAT-O-BALL (October 10, 1990)
  • K900903 — KOPANS HOOKWIRE LESION LOCALIZATION NEEDLE (May 3, 1990)
  • K882628 — ENDO C BRUSH (July 25, 1988)
  • K862410 — MILEX KEGEL PERINEAL EXERCISER (July 31, 1986)
  • K861385 — MILEX BARTHOLIN GLAND CATHETER (June 16, 1986)

Other clearances for product code HHK

  • K251882 — Uterine Aspiration Set (October 16, 2025)
  • K240434 — RELIEEV Suction Curette (Flexible 3.0/ Standard 3.6) (September 25, 2024)
  • K201952 — CrossGlide ETS Plus (August 5, 2020)
  • K192534 — CrossBay Endometrial Tissue Sampler (ETS) (March 25, 2020)
  • K102847 — DISPOSABLE ENDOMETRIAL SUCTION CURETTE (April 14, 2011)
  • K092982 — THE PANPAC SUCTION CURETTE (July 26, 2010)
  • K051294 — FEMTEST ENDOMETRIAL SUCTION CURETTE, MODEL FT-1 (December 21, 2005)
  • K040189 — ENDOMETRIAL SAMPLING SYRINGE (October 4, 2004)
  • K021876 — MAS WITH OR WITHOUT SYRINGE (April 8, 2003)
  • K020628 — CURELLE, PREFERRED CURELLE, CUTEQ 2.5 (May 24, 2002)

FDA data resources