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

ULTRACELL ORTHOPEDIC SPONGES

K Number: K950370 · Decision Apr 17, 1995
Classifications
1
FEI Numbers
228
Registration Numbers
228
Same Product Code
111
Applicant Total
24
Review Days
76

Basic Information

Device Name
ULTRACELL ORTHOPEDIC SPONGES
K Number
K950370
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
ULTRACELL MEDICAL TECHNOLOGIES, INC.
Date Received
January 31, 1995
Decision Date
April 17, 1995
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 ULTRACELL MEDICAL TECHNOLOGIES, INC.

K Number Device Name
K012196 ULTRACELL ABSORBENT STICK
K972633 ULTRACELL SUCTION SPONGE
K972634 ULTRACELL SUCTION SPONGE
K973083 ULTRACELL NEURO SPONGES
K973558 VISUAL ENDOSCOPIC NON-ALCOHOL ULTRACELL SPONGE (VENUS)
K973085 ULTRACELL PACKING WITH SLEEVE
K972635 ULTRACELL SUCTION SPONGE
K970328 ULTRACELL NEURO SPONGES
K950647 ULTRACELL NEURO SPONGES
K950373 ULTRACELL ORTHOPEDIC SPONGES
Search all 24 clearances from ULTRACELL MEDICAL TECHNOLOGIES, INC. →