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

GLUCOMETER ELITE LOW CONTROL

K Number: K940577 · Decision Jun 13, 1994
Classifications
1
FEI Numbers
269
Registration Numbers
269
Same Product Code
492
Applicant Total
145
Review Days
125

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Basic Information

Device Name
GLUCOMETER ELITE LOW CONTROL
K Number
K940577
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Heraeus Kulzer, Inc.
Date Received
February 8, 1994
Decision Date
June 13, 1994
Product Code
JJX
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
JJX Single (Specified) Analyte Controls (Assayed And Unassayed)

Similar 510(k) Clearances

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

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Other Clearances by Heraeus Kulzer, Inc.

K Number Device Name
K091494 FLEXITIME FLOW
K063062 HKBOND 2006
K060994 MONDIAL
K052543 HERACERAM ZIRKONIA
K043504 PALAIMPACT
K043295 VERSYO.DIRECT
K042878 FLEXITIME XTREME
K030052 OSTIM
K040859 HERACERAM PRESS
K040043 NDX-40 ALLOY
Search all 145 clearances from Heraeus Kulzer, Inc. →