FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

V LANCE

K Number: K821440 · Decision Jun 14, 1982
Classifications
1
FEI Numbers
206
Registration Numbers
207
Same Product Code
53
Applicant Total
9
Review Days
32

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Basic Information

Device Name
V LANCE
K Number
K821440
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.4350
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Sharpoint, Inc.
Date Received
May 13, 1982
Decision Date
June 14, 1982
Product Code
HNN
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
HNN Knife, Ophthalmic

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K Number Device Name
K863595 COATED SUTURE NEEDLE
K861947 SURGICAL KNIFE
K840764 EAR KNIVES
K840855 CORNEAL SCLERAL LANCE
K840659 ANTERIOR CAPSULECTOMY CYSTITOME
K840660 POSTERIOR CAPSULOTOMY CYSTITOME
K830522 STAINLESS STEEL SUTURE 316L
K822112 OPHTHALMIC KNIFE