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

UROL-GUANT

K Number: K852295 · Decision Jul 22, 1985
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
60
Applicant Total
8
Review Days
54

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Basic Information

Device Name
UROL-GUANT
K Number
K852295
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Dimension Diagnostics
Date Received
May 29, 1985
Decision Date
July 22, 1985
Product Code
JJW
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
JJW Urinalysis Controls (Assayed And Unassayed)

Similar 510(k) Clearances

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

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Other Clearances by Dimension Diagnostics

K Number Device Name
K863223 DIMENSION-WBG
K861366 ALT-30, 60 AND 100
K854967 CRITIC - SF, ASSAYED
K853943 CRITIC C LEVEL I & II
K844848 IMA-TROL IMMUNOASSAY CONTROL
K844760 UROL-QUAL
K844709 CRITIC-ARS