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

V. MUELLER VITAL SKIN STAPLER

K Number: K851974 · Decision Jun 11, 1985
Classifications
1
FEI Numbers
104
Registration Numbers
104
Same Product Code
18
Applicant Total
31
Review Days
35

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Basic Information

Device Name
V. MUELLER VITAL SKIN STAPLER
K Number
K851974
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4760
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
American V. Mueller
Date Received
May 7, 1985
Decision Date
June 11, 1985
Product Code
GDT
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
GDT Staple, Removable (Skin)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GDT), ordered by most recent decision date.

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Other Clearances by American V. Mueller

K Number Device Name
K873771 HEYER-SCHULTE(R) ONE PIECE SHUNT VENT. CATH. INTRO
K873332 MAXIVAC(TM) CLOSED WOUND SUCTION DRAINAGE SYSTEM
K871685 HEYER-SCHULTE SPETZLER LUMBAR-PERITONEAL SHUNT SYS
K864676 HEYER-SCHULTE HERMETIC EXTERNAL CSF DRAIN. SYSTEM
K862772 V. MUELLER (R) GOOSENECK CIRCULAR STAPLER
K861471 V. MUELLER VITAL CLIP-HEMOSTATIC CLIP
K854568 V. MUELLER PNEUMO-INTESTINAL 15 VASCULAR & 30 STAP
K854049 HEYER-SCHULTE SYRINGO PERITONEAL SHUNT
K851082 V. MUELLER BLOM-SINGER ESOPHAGEAL INSUFFLATION TES
K850947 V-MUELLER INVERTED LINEAR ANASTOMOSIS INSTRUMENTS
Search all 31 clearances from American V. Mueller →