FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

MULTI-SPIKE

K Number: K861203 · Decision Apr 28, 1986
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
39
Applicant Total
10
Review Days
27

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Basic Information

Device Name
MULTI-SPIKE
K Number
K861203
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.4360
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Surgeon Surgical Instrumentation, Inc.
Date Received
April 1, 1986
Decision Date
April 28, 1986
Product Code
KYG
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

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

Product Code Device Name
KYG Device, Irrigation, Ocular Surgery

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KYG), ordered by most recent decision date.

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Other Clearances by Surgeon Surgical Instrumentation, Inc.

K Number Device Name
K954241 SURGIN GENISIS PHACOEMULSIFIER
K932281 VERRES NEEDLE
K922038 CO2 INSUFFLATION TUBING
K904010 SURGICAL ASPIRATOR KIT
K890447 HEMORRHAGE OCCLUDOR
K880543 UNI-PORT
K881232 SURGIN EYE SHIELD
K852229 STERILE EYE PACKS OR TRAYS
K830859 I/A KIT