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

HEYER-SCHULTE AFTERLOADING CATHETER

K Number: K832738 · Decision Sep 29, 1983
Classifications
1
FEI Numbers
47
Registration Numbers
47
Same Product Code
35
Applicant Total
13
Review Days
48

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Basic Information

Device Name
HEYER-SCHULTE AFTERLOADING CATHETER
K Number
K832738
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.5650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
American Heyer Schulte
Date Received
August 12, 1983
Decision Date
September 29, 1983
Product Code
IWJ
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
IWJ System, Applicator, Radionuclide, Manual

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K833502 RADOVAN SUBCUTANEOUS TISSUE EXPANDER
K833698 AMER. V. MUELLER SURG. STAPLES ILA
K833704 AMER. V. MUELLER SURGICALSTAPLES-CARTR
K823790 VENTRICULAR ACCESS SYSTEM
K822096 CHEMOTHERAPY INFUSION CATHETER
K822032 LARGE VOLUME CLOSED WOUND SUCTION DRAIN
K820247 EXTERNAL VENTRICULAR DRAINAGE SYS.
K811288 SPETZLER LUMBAR-PERITONEAL SYSTEM
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