FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

SOFT PLUG ABSORBABLE PLUG-SA

K Number: K013613 · Decision Jun 27, 2002
Classifications
1
FEI Numbers
37
Registration Numbers
38
Same Product Code
48
Applicant Total
17
Review Days
234

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Basic Information

Device Name
SOFT PLUG ABSORBABLE PLUG-SA
K Number
K013613
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Oasis Medical, Inc.
Date Received
November 5, 2001
Decision Date
June 27, 2002
Product Code
LZU
Advisory Committee
Unknown
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
LZU Plug, Punctum

Similar 510(k) Clearances

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Other Clearances by Oasis Medical, Inc.

K Number Device Name
K213988 SOFT PLUG Extended Duration 180 Tapered Canalicular Plug
K162361 Soft Plug Extended Duration 180 Canalicular Plug
K032297 DISPOSABLE N-PE MICKROKERATOME BLADES
K030401 DISPOSABLE M2-PE MICROKERATOME BLADES
K022205 DISPOSABLE N-PE MICROKERATOME BLADES
K003820 DISPOSABLE CB-PE MICROKERATOME BLADES
K001176 DISPOSABLE MICROKERATOME BLADES-PE
K980437 SILICONE PUNCTAL PLUG
K950798 POSTERIOR CAPSULE SHIELD
K950241 OPHTHALMIC SPONGES
Search all 17 clearances from Oasis Medical, Inc. →