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

ISOLATION MASKS

K Number: K893939 · Decision Jul 14, 1989
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
606
Applicant Total
15
Review Days
44

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Basic Information

Device Name
ISOLATION MASKS
K Number
K893939
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4040
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
James River Corp.
Date Received
May 31, 1989
Decision Date
July 14, 1989
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 James River Corp.

K Number Device Name
K894505 COTOLIN DRAIN SPONGE AND DRESSING SPONGE
K894147 VISULIN TRANSPARENT ADHESIVE DRESSING
K894034 MODIFIED LABELING OF SURGICAL GLOVES
K892580 CARETOUCH EXAMINATION GLOVES
K890459 JAMES RIVER BIOGEL POWDERLESS SURGICAL GLOVES
K883802 CARETEX CENTRAL SUPPLY WRAP
K884112 CARETEX OR TOWEL
K883657 SKID RESISTANT, LONG LASTING SHOE COVERS
K880431 CARETEX SURGEON'S HOODS
K880481 CARETEX SURGEON'S CAPS
Search all 15 clearances from James River Corp. →