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

LASERSAFE EYE SHIELDS

K Number: K852404 · Decision Oct 4, 1985
Classifications
1
FEI Numbers
712
Registration Numbers
712
Same Product Code
54
Applicant Total
3
Review Days
120

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Basic Information

Device Name
LASERSAFE EYE SHIELDS
K Number
K852404
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.4750
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Lasersafe, Inc.
Date Received
June 6, 1985
Decision Date
October 4, 1985
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 Lasersafe, Inc.

K Number Device Name
K854266 STERILE LASER RESISTANT SURGICAL FIELD DRAPE
K852405 LASERSAFE PERSONNEL AND PATIENT SHIELDS