FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

GLUCOLET AUTOMATIC LANCING DEVICE FOR OBT. BLOOD

K Number: K855203 · Decision Feb 11, 1986
Classifications
1
FEI Numbers
157
Registration Numbers
157
Same Product Code
109
Applicant Total
158
Review Days
47

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Basic Information

Device Name
GLUCOLET AUTOMATIC LANCING DEVICE FOR OBT. BLOOD
K Number
K855203
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4850
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Miles Laboratories, Inc.
Date Received
December 26, 1985
Decision Date
February 11, 1986
Product Code
FMK
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
FMK Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature

Similar 510(k) Clearances

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

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Other Clearances by Miles Laboratories, Inc.

K Number Device Name
K880605 LABELING CHANGE FOR CUTTER PUREFLO PLUS IV FILTER
K874909 MICRO-BUMINTEST REAGENT TABLETS
K875079 MODIFIED SERALYZER ALT/SGPT REAG. STRIPS & MODULE
K871835 GLUCOMETER QC BLOOD METER, AMES GLUCO SYSTEM PRINT
K872120 SERALYZER III BLOOD CHEMISTRY ANALYZER
K873304 CLINITEK AUTO 2000 REAGENT CASSETTE (LEUKOCYTES)
K872634 CUTTER PUREFLO PLUS IV FILTER
K870214 MODIFIED SALTEX REAGENT STRIPS
K870752 SERALYZER LDH/TOTAL BILIRUBIN/TRIGLYCERIDES STRIPS
K865053 SERA-TEK MICROSOMAL ANTIBODY TEST
Search all 158 clearances from Miles Laboratories, Inc. →