ClearanceBrief
Company ยท US

Lukens Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1977 to 1988. Name variants (Inc, Corp, punctuation) are merged.

11510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
GDYGauze/Sponge, Internal, X-Ray Detectable2
GESBlade, Scalpel2
KKXDrape, Surgical, Antimicrobial2
FRGWrap, Sterilization1
IKKSystem, Isokinetic Testing And Evaluation1
JJXSingle (Specified) Analyte Controls (Assayed And Unassayed)1
KDCInstrument, Surgical, Disposable1
MTJWax, Bone1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Mar 16, 1988K880230SIXALYZER
Lukens Corp.
IKK
Jan 28, 1980K800102STANFORD STERILE LAP SPONGES
Lukens Corp.
GDY
Dec 20, 1979K792471STANFORD STERILE LAP SPONGES
Lukens Corp.
GDY
Sep 24, 1979K791495LUKENS BONE WAX (GAMMA RADIATION)
Lukens Corp.
MTJ
Jul 11, 1977K770797TRAY, CATHETERIZATION W/FOLEY, STERILE
Lukens Corp.
FRG
Jul 11, 1977K770795SHAVE PREP SET
Lukens Corp.
JJX
Jun 22, 1977K770799TRAY, IRRIGATION, STERILE, BASIC
Lukens Corp.
KKX
Jun 22, 1977K770796SKIN SCRUB PREP SET
Lukens Corp.
KKX
May 6, 1977K770800HANDLES, BLADE, SURGICAL
Lukens Corp.
GES
May 6, 1977K770798BLADES, SURGICAL, STERILE
Lukens Corp.
GES
May 6, 1977K770794SUTURE REMOVAL SET, STERILE
Lukens Corp.
KDC

Latest recalls

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