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

780 nm SPY Portable Handheld Imaging (SPY-PHI) System

K Number: K261037 · Decision May 28, 2026
Classifications
1
FEI Numbers
123
Registration Numbers
123
Same Product Code
198
Applicant Total
101
Review Days
59

Basic Information

Device Name
780 nm SPY Portable Handheld Imaging (SPY-PHI) System
K Number
K261037
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1600
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stryker Endoscopy
Date Received
March 30, 2026
Decision Date
May 28, 2026
Product Code
IZI
Advisory Committee
Radiology
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
IZI System, X-Ray, Angiographic

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