FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

ISOLYSER (8X4 12 PLY X-RAY DETECTABLE)

K Number: K940763 · Decision May 2, 1994
Classifications
1
FEI Numbers
211
Registration Numbers
211
Same Product Code
110
Applicant Total
21
Review Days
73

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Basic Information

Device Name
ISOLYSER (8X4 12 PLY X-RAY DETECTABLE)
K Number
K940763
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4450
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Thantex Specialties, Inc.
Date Received
February 18, 1994
Decision Date
May 2, 1994
Product Code
GDY
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
GDY Gauze/Sponge, Internal, X-Ray Detectable

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Other Clearances by Thantex Specialties, Inc.

K Number Device Name
K970547 ISOLYSER SDS SHARPS CONTAINER
K961083 OREX SURGEON'S VEST
K942200 ISOLYSER OREX SURGEON'S CAPS, HOODS, BOUFFANT CAPS
K943626 ISOLYSER SHARPS MANAGEMENT SYSTEM SMS
K945755 OREX(R) O.R EQUIPMENT DRAPES
K945223 OREX ISOLATION GOWN
K944859 OREX SURGICAL DRAPES
K944827 OREX SURGEON'S GOWN
K943034 OREX SHOE COVERS
K942228 OREX O.R. TOWEL
Search all 21 clearances from Thantex Specialties, Inc. →