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

BOSTON ES MULTIVISION (ENFLUFOCON A) CONTACT LENS

K Number: K970698 · Decision May 6, 1997
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
117
Applicant Total
23
Review Days
70

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Basic Information

Device Name
BOSTON ES MULTIVISION (ENFLUFOCON A) CONTACT LENS
K Number
K970698
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.5916
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Polymer Technology Corp.
Date Received
February 25, 1997
Decision Date
May 6, 1997
Product Code
HQD
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
HQD Lens, Contact (Other Material) - Daily

Similar 510(k) Clearances

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Other Clearances by Polymer Technology Corp.

K Number Device Name
K011945 RIGID GAS PERMEABLE CONTACT LENS SOLUTION
K980133 BAUSCH & LOMB WETTING AND SOAKING SOLUTION
K974466 BOSTON ADVANCE CLEANER
K973217 BOSTON LIQUID ENZYMATIC CLEANER
K951552 BOSTON CONTACT LENS CASE
K943177 BOSTON(R) 7 - 30(ENFLUFOCON A)
K942365 BOSTON VII
K923438 BOSTON CONDITIONING SOLUTION
K923587 GLUCOSE TEST SYSTEM
K923437 BOSTON CLEANER II
Search all 23 clearances from Polymer Technology Corp. →