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

ARKIVE (TM)

K Number: K862085 · Decision Jan 12, 1987
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
187
Applicant Total
15
Review Days
224

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Basic Information

Device Name
ARKIVE (TM)
K Number
K862085
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5160
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Diatek, Inc.
Date Received
June 2, 1986
Decision Date
January 12, 1987
Product Code
BSZ
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
BSZ Gas-Machine, Anesthesia

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Other Clearances by Diatek, Inc.

K Number Device Name
K020430 DIATEK CONNECTOR ASSEMBLY REPLACEMENT KIT (CARK)
K010399 DIATEK CANNON-CATH #CC2400, CC2800, CC3200, CC3600,CC5500. CC2400PC, CC2800PC, CC3200PC(32 CM), CC3200PC(36 CM)
K895703 DIATEK MODEL 700 THERMOMETER
K872178 MODIFICATION TO ARKIVE(TM)
K841827 ENTEROPORT NUTRITION PUMP
K841859 SECURA SET
K833568 DIATEK 600 THERMOMETER SYSTEM
K830565 SECURA SET SECONDARY ADMIN. SET
K830377 SECURA SET PRIMARY ADMIN. SET
K830355 SECURA IV VOLUMETRIC INFUSION PUMP
Search all 15 clearances from Diatek, Inc. →