FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

SAVETT ALCOHOL PREP

K Number: K830330 · Decision Mar 17, 1983
Classifications
1
FEI Numbers
113
Registration Numbers
113
Same Product Code
24
Applicant Total
7
Review Days
44

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Basic Information

Device Name
SAVETT ALCOHOL PREP
K Number
K830330
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Applicant
Cederroth, Inc. USA
Date Received
February 1, 1983
Decision Date
March 17, 1983
Product Code
LKB
Advisory Committee
Unknown
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
LKB Pad, Alcohol, Device Disinfectant

Similar 510(k) Clearances

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

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Other Clearances by Cederroth, Inc. USA

K Number Device Name
K880788 NON ADHERENT PAD
K823057 MEDICATED ADHESIVE STRIP
K820059 RESUSCITATION MASK
K813365 MULTIPLE BANDAGE OR DRESSING
K813364 MEDICAL TAPE (MULTIPLE)
K813361 ADHESIVE STRIP(MULTIPLE)