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

LKB-BROMMA 2218 HISTORANGE MICROTOME

K Number: K812157 · Decision Aug 18, 1981
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
4
Applicant Total
52
Review Days
20

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Basic Information

Device Name
LKB-BROMMA 2218 HISTORANGE MICROTOME
K Number
K812157
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.3010
Medical Specialty
Pathology
Decision
Substantially Equivalent
Applicant
Lkb Instruments, Inc.
Date Received
July 29, 1981
Decision Date
August 18, 1981
Product Code
IDO
Advisory Committee
Pathology
Review Advisory Committee
HE
Third Party
N

Classifications

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

Product Code Device Name
IDO Microtome, Rotary

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K871599 DELFIA(TM) HIGE KIT
K871644 DELFIA (TM) HTSH KIT
K864452 DELFIA(TM) TRIIODOTHYRONINE (T3) KIT
K864733 LKB 2260 MACROTOME
K862848 LKB ULTROBACT (TM) PNEUMOCOCCUS KIT; 2321-110
K863422 DELFIA(TM) CORTISOL KIT
K861195 DELFIA DIGOXIN
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