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

BOSTON CONTACT LENS CASE

K Number: K951552 · Decision Jun 26, 1995
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
81
Applicant Total
23
Review Days
83

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Basic Information

Device Name
BOSTON CONTACT LENS CASE
K Number
K951552
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.5928
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Polymer Technology Corp.
Date Received
April 4, 1995
Decision Date
June 26, 1995
Product Code
LRX
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
LRX Case, Contact Lens

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Other Clearances by Polymer Technology Corp.

K Number Device Name
K011945 RIGID GAS PERMEABLE CONTACT LENS SOLUTION
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K974466 BOSTON ADVANCE CLEANER
K973217 BOSTON LIQUID ENZYMATIC CLEANER
K970698 BOSTON ES MULTIVISION (ENFLUFOCON A) CONTACT LENS
K943177 BOSTON(R) 7 - 30(ENFLUFOCON A)
K942365 BOSTON VII
K923438 BOSTON CONDITIONING SOLUTION
K923587 GLUCOSE TEST SYSTEM
K923437 BOSTON CLEANER II
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