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

MEDPOR COATED TEAR DRAIN

K Number: K012108 · Decision Dec 19, 2001
Classifications
1
FEI Numbers
20
Registration Numbers
21
Same Product Code
30
Applicant Total
19
Review Days
166

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Basic Information

Device Name
MEDPOR COATED TEAR DRAIN
K Number
K012108
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Porex Surgical, Inc.
Date Received
July 6, 2001
Decision Date
December 19, 2001
Product Code
OKS
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
OKS Lacrimal Stents And Intubation Sets

Similar 510(k) Clearances

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Other Clearances by Porex Surgical, Inc.

K Number Device Name
K102184 MEDPOR CONTAIN CAN IMPLANT
K101835 MEDPOR FIXATION SYSTEM-CRANIAL, MODELS 80080, 80079
K091807 MEDPOR FIXATION SYSTEM
K091120 MEDPOR CONTAIN IMPLANT
K083621 MEDPOR CUSTOMIZED SURGICAL IMPLANT
K071335 MEDPOR ATTRACTOR IMPLANT
K052297 POREX ELECTROSURGERY NEEDLE
K040851 MEDPOR ATTRACTOR MAGNETIC COUPLING SYSTEM
K040364 MEDPOR CRANIOFACIAL IMPLANTS WITH EMBEDDED TITANIUM MESH
K021357 MEDPOR PLUS ORBITAL VOLUME REPLACEMENT IMPANT
Search all 19 clearances from Porex Surgical, Inc. →