510(k) K233635

SPY Cystoscope/Hysteroscope by Stryker Endoscopy — Product Code HIH

K233635 is an FDA 510(k) premarket notification submitted by Stryker Endoscopy for the device "SPY Cystoscope/Hysteroscope". The FDA issued a decision of Substantially Equivalent on February 12, 2024. The device falls under product code HIH (Hysteroscope (And Accessories)), a Class II device regulated under 21 CFR 884.1690. Stryker Endoscopy has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 12, 2024
Date Received
November 13, 2023
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Hysteroscope (And Accessories)
Device Class
Class II
Regulation Number
884.1690
Review Panel
OB
Submission Type