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

DUJOVNY MICROSURGICAL SCISSORS

K Number: K810485 · Decision Feb 27, 1981
Classifications
1
FEI Numbers
136
Registration Numbers
136
Same Product Code
12
Applicant Total
31
Review Days
4

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Basic Information

Device Name
DUJOVNY MICROSURGICAL SCISSORS
K Number
K810485
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
882.4525
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
American V. Mueller
Date Received
February 23, 1981
Decision Date
February 27, 1981
Product Code
GZX
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
GZX Instrument, Microsurgical

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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 →