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510(k) K812175

ENDOCERVICAL ASPIRATOR by Fertility Instrumentation, Inc. — Product Code HFC

K812175 is an FDA 510(k) premarket notification submitted by Fertility Instrumentation, Inc. for the device "ENDOCERVICAL ASPIRATOR". The FDA issued a decision of Substantially Equivalent on September 21, 1981. The device falls under product code HFC (Aspirator, Endocervical), a Class II device regulated under 21 CFR 884.1050.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 21, 1981
Date Received
August 3, 1981
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Aspirator, Endocervical
Device Class
Class II
Regulation Number
884.1050
Review Panel
OB
Submission Type

Other clearances for product code HFC

  • K974032 — ROCKET MUCUS SAMPLER SYRINGE, STERILE, ROCKET MUCUS SAMPLER SYRINGE, CLINICALLY (December 22, 1997)
  • K960263 — CERVICAL MUCOUS ASPIRATION CATHETER (August 29, 1996)
  • K954903 — PEDI VAGINAL ASPIRATOR (April 29, 1996)
  • K954102 — SELECTMUCUS (November 21, 1995)
  • K902242 — ENDOCERVICAL ASPIRATOR (October 9, 1990)
  • K902032 — O. B. PACK IV (September 28, 1990)
  • K902954 — OBER2 MONITOR, EYE MOVEMENT (OPHTHALMIC) (August 23, 1990)
  • K895403 — ASPIRETTE ENDOCERVICAL ASPIRATOR (November 29, 1989)
  • K821134 — DC PACK TM (June 22, 1982)
  • K801238 — ACCU-PAP T ZONE SAMPLER (August 12, 1980)

FDA data resources