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

ACUCAM INTRAORAL CAMERA SHEATHS, MODELS 023545, 601111, 300407, 601285

K Number: K994211 · Decision Feb 4, 2000
Classifications
1
FEI Numbers
200
Registration Numbers
200
Same Product Code
449
Applicant Total
279
Review Days
52

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Basic Information

Device Name
ACUCAM INTRAORAL CAMERA SHEATHS, MODELS 023545, 601111, 300407, 601285
K Number
K994211
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4370
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dentsply Intl.
Date Received
December 14, 1999
Decision Date
February 4, 2000
Product Code
KKX
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
KKX Drape, Surgical, Antimicrobial

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