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

STERI-CATH-DL

K Number: K902687 · Decision Aug 29, 1990
Classifications
1
FEI Numbers
245
Registration Numbers
245
Same Product Code
115
Applicant Total
23
Review Days
71

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Basic Information

Device Name
STERI-CATH-DL
K Number
K902687
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.6810
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Concord/Portex
Date Received
June 19, 1990
Decision Date
August 29, 1990
Product Code
BSY
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
BSY Catheters, Suction, Tracheobronchial

Similar 510(k) Clearances

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

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Other Clearances by Concord/Portex

K Number Device Name
K923559 STERI-CATH MDI
K930218 SUBCUTANEOUS TUNNELING NEEDLE AND HANDLES
K924541 EPIDURAL MINIPACK
K930286 DRI-VENDT/PROVENT/ACCUVENT ARTERIAL BLOOD GAS KITS
K923127 NEEDLE-PRO CARTRIDGE
K923910 HEAT MOISTURE CONDENSER
K922749 LOW PROFILE TRACHEOSTOMY TUBE
K922445 VACU-PRO
K915452 ANESTHESIA BREATHING CIRCUIT
K911809 NEW-VENT
Search all 23 clearances from Concord/Portex →