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

Paneffort 3-ply Surgical and Procedural Masks

K Number: K221409 · Decision Jul 25, 2022
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
606
Applicant Total
2
Review Days
70

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Basic Information

Device Name
Paneffort 3-ply Surgical and Procedural Masks
K Number
K221409
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4040
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Paneffort, LLC
Date Received
May 16, 2022
Decision Date
July 25, 2022
Product Code
FXX
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
FXX Mask, Surgical

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Other Clearances by Paneffort, LLC

K Number Device Name
K212717 Paneffort AAMI Level 3 Isolation Gown