ClearanceBrief
Company ยท US

American White Cross, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1985 to 1997. Name variants (Inc, Corp, punctuation) are merged.

10510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
KGXTape And Bandage, Adhesive2
EFQGauze/Sponge, Internal1
FPXStrip, Adhesive, Closure, Skin1
KMFBandage, Liquid1
LWFDilator, Nasal1
NADDressing, Wound, Occlusive1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Feb 6, 1997K964614ULTRAFERA WOUND DRESSING
American White Cross, Inc.
KMF
Sep 9, 1996K962400AIR MAX EXTERNAL NASAL DILATOR STRIP
American White Cross, Inc.
LWF
Jan 31, 1990K894802AWC BUTTERFLY WOUND CLOSURES
American White Cross, Inc.
FPX
Jan 13, 1986K854809WHITE CROSS STERILE PAD 4IN. X 4IN.
American White Cross, Inc.
Sep 5, 1985K853558DOSIMETRIC RELEASE/RADIATION STERILIZ. ABSORB GAUZ
American White Cross, Inc.
Aug 21, 1985K853334NON-ADHERA ADHESIVE PAD 3X4
American White Cross, Inc.
NAD
Jul 29, 1985K852412NON-ADHERENT PAD
American White Cross, Inc.
EFQ
Jul 29, 1985K852408EXTRA LARGE ADHESIVE STRIPS
American White Cross, Inc.
KGX
Jul 26, 1985K852462TRICOT ADHESIVE BANDAGE
American White Cross, Inc.
KGX
Mar 11, 1985K8505953 X 4 NON-ADHERENT PAD
American White Cross, Inc.

Latest recalls

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