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

RETRACTING PROBES

K Number: K811759 · Decision Jul 20, 1981
Classifications
1
FEI Numbers
656
Registration Numbers
656
Same Product Code
99
Applicant Total
31
Review Days
28

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Basic Information

Device Name
RETRACTING PROBES
K Number
K811759
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
American V. Mueller
Date Received
June 22, 1981
Decision Date
July 20, 1981
Product Code
GAD
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
GAD Retractor

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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 →