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

SURELOC CIRCUIT CONNECTOR

K Number: K954383 · Decision Dec 22, 1995
Classifications
1
FEI Numbers
167
Registration Numbers
167
Same Product Code
93
Applicant Total
20
Review Days
94

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Basic Information

Device Name
SURELOC CIRCUIT CONNECTOR
K Number
K954383
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5810
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Polamedco, Inc.
Date Received
September 19, 1995
Decision Date
December 22, 1995
Product Code
BZA
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
BZA Connector, Airway (Extension)

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Other Clearances by Polamedco, Inc.

K Number Device Name
K983000 CRICOTHYROTOMY TUBE
K953793 INTROSCOPE
K950713 AIRGUIDE STYLETTE
K933596 GASTRIC, CATHETER, IRRIGATION & ASPIRATION
K950380 FLEXTITIP STYLETTE
K920900 POLAMEDCO TRACHEAL AND NASOTRACHEAL TUBES
K900456 POLAMEDCO NASOPAHARYNGEAL AIRWAY
K900457 CUFFED LINDER NASOTRACHEAL AIRWAY
K894516 VISOSHIELD(TM), SURGICAL EYE PROTECTOR
K881496 LINDER NASOTRACHEAL AIRWAY
Search all 20 clearances from Polamedco, Inc. →