510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K845009Substantially Equivalent

Rabbit-Personal Computer for Women

Sanimor, Inc., Beverly Hills CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K845009 is the FDA 510(k) clearance record for RABBIT-PERSONAL COMPUTER FOR WOMEN, cleared for Sanimor, Inc. on under FDA product code LHD (Device, Fertility Diagnostic, Proceptive). FDA records list one 510(k) clearance for Sanimor, Inc. As of , FDA records show no recalls naming K845009.

Clearance record

Decision date
Received
(105 days to decision)
Product code
LHD Device, Fertility Diagnostic, Proceptive
Device class
Unclassified
Review panel
Unknown
Applicant
Sanimor, Inc. 144 S. Beverly Dr., Beverly Hills CA
Third party review
No

Clearances, product code LHD

Trailing 12 months

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

FDA records show no clearances under product code LHD in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LHD, 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