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

MARTIN TRACH-SECURE

K Number: K810575 · Decision Mar 17, 1981
Classifications
1
FEI Numbers
74
Registration Numbers
74
Same Product Code
127
Applicant Total
15
Review Days
14

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Basic Information

Device Name
MARTIN TRACH-SECURE
K Number
K810575
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5800
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Diatek, Inc.
Date Received
March 3, 1981
Decision Date
March 17, 1981
Product Code
BTO
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
BTO Tube, Tracheostomy (W/Wo Connector)

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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)
K862085 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
Search all 15 clearances from Diatek, Inc. →