510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K983181Substantially Equivalent

Cytoprep

Cytoprep Inc. Est., Eschen, LI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K983181 is the FDA 510(k) clearance record for CYTOPREP, a class II device, cleared for Cytoprep Inc. Est. on under FDA product code HHI (System, Abortion, Vacuum). FDA records list one 510(k) clearance for Cytoprep Inc. Est. As of , FDA records show no recalls naming K983181.

Clearance record

Decision date
Received
(66 days to decision)
Product code
HHI System, Abortion, Vacuum
Regulation
21 CFR 884.5070
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Cytoprep Inc. Est. Renkwiler 593, Eschen, LI
510(k) summary
Summary
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