CONCHA-COLUMN

Humidifier, Respiratory Gas, (direct Patient Interface)

RESPIRATORY CARE, INC.

The following data is part of a premarket notification filed by Respiratory Care, Inc. with the FDA for Concha-column.

Pre-market Notification Details

• Device ID: K760866
• 510k Number: K760866
• Device Name: CONCHA-COLUMN
• Classification: Humidifier, Respiratory Gas, (direct Patient Interface)
• Applicant: RESPIRATORY CARE, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050
• Product Code: BTT
• CFR Regulation Number: 868.5450 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1976-10-18
• Decision Date: 1976-11-01

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
14026704611383	K760866	000
14026704396310	K760866	000
14026704396341	K760866	000
14026704396365	K760866	000
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24026704396188	K760866	000
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14026704396297	K760866	000
14026704396242	K760866	000
34026704734017	K760866	000
34026704734031	K760866	000
34026704734048	K760866	000
34026704659471	K760866	000
34026704659532	K760866	000
14026704659583	K760866	000
34026704659594	K760866	000
14026704396235	K760866	000
24026704659429	K760866	000
24026704659436	K760866	000
34026704628187	K760866	000
34026704628217	K760866	000
34026704628262	K760866	000
14026704628305	K760866	000
14026704628312	K760866	000
34026704628637	K760866	000
24026704610710	K760866	000
34026704611356	K760866	000
24026704659597	K760866	000
24026704659573	K760866	000
24026704659474	K760866	000
24026704659481	K760866	000
24026704659498	K760866	000
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24026704659542	K760866	000
24026704659566	K760866	000
34026704734000	K760866	000