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

CIRCLE NEPHROSTOMY TUBE INTRODUCER

K Number: K810533 · Decision Mar 11, 1981
Classifications
1
FEI Numbers
113
Registration Numbers
113
Same Product Code
43
Applicant Total
31
Review Days
13

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Basic Information

Device Name
CIRCLE NEPHROSTOMY TUBE INTRODUCER
K Number
K810533
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
876.4730
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
American V. Mueller
Date Received
February 26, 1981
Decision Date
March 11, 1981
Product Code
KOA
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KOA Surgical Instruments, G-U, Manual (And Accessories)

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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
K851974 V. MUELLER VITAL SKIN STAPLER
Search all 31 clearances from American V. Mueller →