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

MODIFIED PARACON(TM) CONCENTRATION KIT

K Number: K881649 · Decision Apr 21, 1988
Classifications
1
FEI Numbers
6
Registration Numbers
6
Same Product Code
12
Applicant Total
5
Review Days
6

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Basic Information

Device Name
MODIFIED PARACON(TM) CONCENTRATION KIT
K Number
K881649
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2900
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Para Scientific Co.
Date Received
April 15, 1988
Decision Date
April 21, 1988
Product Code
LKS
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

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

Product Code Device Name
LKS Device, Parasite Concentration

Similar 510(k) Clearances

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

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Other Clearances by Para Scientific Co.

K Number Device Name
K021420 PARACON II/FECAL CONCENTRATOR II
K964144 PARACON PLUS FORMALIN - PCP-F, PARACON PLUS SAF - PCP-SAF AND PARACON PLUS MF - PCP-MF
K872751 FLUORTRAN - C(TM)
K853715 PARA CON TM