510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K870999Substantially Equivalent

Gender Choice Information Kit, Female and Male

Procare C/O Wiley, Rein & Fielding, Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K870999 is the FDA 510(k) clearance record for GENDER CHOICE INFORMATION KIT, FEMALE AND MALE, cleared for Procare C/O Wiley, Rein & Fielding on under FDA product code LHD (Device, Fertility Diagnostic, Proceptive). FDA records list one 510(k) clearance for Procare C/O Wiley, Rein & Fielding. As of , FDA records show no recalls naming K870999.

Clearance record

Decision date
Received
(125 days to decision)
Product code
LHD Device, Fertility Diagnostic, Proceptive
Device class
Unclassified
Review panel
Unknown
Applicant
Procare C/O Wiley, Rein & Fielding 1776 K St. NW, Washington DC
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