510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K850312Substantially Equivalent

Gynaspyr Vacuum Curettage Unit

Roseburg SA, Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K850312 is the FDA 510(k) clearance record for GYNASPYR VACUUM CURETTAGE UNIT, a class II device, cleared for Roseburg SA on under FDA product code HHI (System, Abortion, Vacuum). FDA records list 24 510(k) clearances for Roseburg SA, from to . As of , FDA records show no recalls naming K850312.

Clearance record

Decision date
Received
(34 days to decision)
Product code
HHI System, Abortion, Vacuum
Regulation
21 CFR 884.5070
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Roseburg SA 1054 31st St., NW, Washington DC
Third party review
No

Clearances, product code HHI

Trailing 12 months

FDA records hold no clearances under product code HHI in the trailing twelve months.

FDA records show no clearances under product code HHI in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HHI, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260