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

EYE SPEAR

K Number: K840471 · Decision Mar 16, 1984
Classifications
1
FEI Numbers
77
Registration Numbers
78
Same Product Code
46
Applicant Total
19
Review Days
42

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Basic Information

Device Name
EYE SPEAR
K Number
K840471
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4790
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Surgicot, Inc.
Date Received
February 3, 1984
Decision Date
March 16, 1984
Product Code
HOZ
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
HOZ Sponge, Ophthalmic

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K854631 ASSERT EO BIOLOGICAL TEST PACK
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K840541 NEURO SPONGE
K840470 SURGISCRIBE MARKING PEN
K830739 PRO-GUARD
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