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

ScanX Barrier Envelopes

K Number: K190949 · Decision Jul 26, 2019
Classifications
1
FEI Numbers
48
Registration Numbers
48
Same Product Code
14
Applicant Total
18
Review Days
106

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Basic Information

Device Name
ScanX Barrier Envelopes
K Number
K190949
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
Air Techniques, Inc.
Date Received
April 11, 2019
Decision Date
July 26, 2019
Product Code
PEM
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
PEM Dental Barriers And Sleeves

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (PEM), ordered by most recent decision date.

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Other Clearances by Air Techniques, Inc.

K Number Device Name
K191623 ScanX Touch/ScanX Duo Touch
K101289 SCANX D5000 SERIES SCANNER MODEL: D5000-F, D5000-FB, D5000-FVB, D5000-Q, D5000-QB
K090169 SPECTRA FLUORESCENCE CARIES DETECTION DEVICE
K052271 RINSENDO
K050693 ACCENT
K042397 SCANX 14
K042266 ACCLAIM
K031198 SCANX 10
K024285 A/T X-RAY 70
K013893 SCANX
Search all 18 clearances from Air Techniques, Inc. →