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

LANCET, BLOOD

K Number: K883420 · Decision Aug 26, 1988
Classifications
1
FEI Numbers
157
Registration Numbers
157
Same Product Code
109
Applicant Total
14
Review Days
11

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Basic Information

Device Name
LANCET, BLOOD
K Number
K883420
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4850
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Primrose Medical, Inc.
Date Received
August 15, 1988
Decision Date
August 26, 1988
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 Primrose Medical, Inc.

K Number Device Name
K884714 BILIARY DIALATOR
K884715 ACHELASIA BALLOON DIALATOR
K884713 COLONIC BALLOON DIALATORS
K884711 URETHRAL AND URETERAL BALLOON DILATATORS
K884709 ENDOSCOPES & ACCESS.(SCLEROTHERAPY/TRANSBRONCHIAL)
K884712 ESOPHAGEAL AND PYLORIC BALLOON DIALATORS
K881976 CATHETER, INTRAVASCULAR
K881977 PRESSURE INFUSOR
K881975 SET, INTRAVASCULAR
K881978 ENTERAL FEEDING TUBES
Search all 14 clearances from Primrose Medical, Inc. →