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Parker Quality & Compliance

PQC Reg Watch

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510(k) clearance

Cyperus

FDA 510(k) source

510(k) number
K262276
Applicant
Contrario Medical, Inc.
Decision date
Oct 26, 2026
Date received
Jul 6, 2026
Decision
Substantially Equivalent
Clearance type
Traditional
Product code
MQK
Device type
Labware, Assisted Reproduction
Device class
Class II
Regulation
21 CFR 884.6160
Advisory committee
Obstetrics/Gynecology
Statement or summary
Summary
Third party
N
Location
Houston, TX, US