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

SNJ SMOKE EVACUATION SUCTION WAND

K Number: K935439 · Decision Mar 7, 1994
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
74
Applicant Total
12
Review Days
115

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Basic Information

Device Name
SNJ SMOKE EVACUATION SUCTION WAND
K Number
K935439
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.5070
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Lca, Inc.
Date Received
November 12, 1993
Decision Date
March 7, 1994
Product Code
FYD
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FYD Apparatus, Exhaust, Surgical

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Other Clearances by Lca, Inc.

K Number Device Name
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K935258 HYBRID SURGICAL DEVICE MODIFICATION
K925726 ALLOY SCALPEL HANDPIECES, MODIFICATION
K931070 CLOSED END FIBEROPTIC LASER DELIVERY SYSTEM
K924160 HYBRID SURGICAL DEVICE
K923991 ZOE LASER, CONTACT ND:YAG LASER SYSTEM
K924120 MOLDED FIBER CAP DELIVERY SYSTEM
K901365 LASER FORCEPS HANDPIECE
K902562 REVISED LABELING FOR MODEL CL-0PE ND:YAG LASER
Search all 12 clearances from Lca, Inc. →