FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SPY Cystoscope/Hysteroscope

K Number: K252012 · Decision Jul 18, 2025
Classifications
1
FEI Numbers
135
Registration Numbers
135
Same Product Code
170
Applicant Total
101
Review Days
21

Basic Information

Device Name
SPY Cystoscope/Hysteroscope
K Number
K252012
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
884.1690
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stryker Endoscopy
Date Received
June 27, 2025
Decision Date
July 18, 2025
Product Code
HIH
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HIH Hysteroscope (And Accessories)

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