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

SURGIN EYE SHIELD

K Number: K881232 · Decision Apr 13, 1988
Classifications
1
FEI Numbers
712
Registration Numbers
712
Same Product Code
54
Applicant Total
10
Review Days
22

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Basic Information

Device Name
SURGIN EYE SHIELD
K Number
K881232
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.4750
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Surgeon Surgical Instrumentation, Inc.
Date Received
March 22, 1988
Decision Date
April 13, 1988
Product Code
HOY
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
HOY Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HOY), 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
K861203 MULTI-SPIKE
K852229 STERILE EYE PACKS OR TRAYS
K830859 I/A KIT