510(k) K870332

PREFILLED RESPIRATORY THERAPY VIALS by Automatic Liquid Packaging, Inc. — Product Code CCQ

K870332 is an FDA 510(k) premarket notification submitted by Automatic Liquid Packaging, Inc. for the device "PREFILLED RESPIRATORY THERAPY VIALS". The FDA issued a decision of Substantially Equivalent on April 1, 1987. The device falls under product code CCQ (Nebulizer, Medicinal, Non-Ventilatory (Atomizer)), a Class I device regulated under 21 CFR 868.5640. Automatic Liquid Packaging, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 1, 1987
Date Received
January 28, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Nebulizer, Medicinal, Non-Ventilatory (Atomizer)
Device Class
Class I
Regulation Number
868.5640
Review Panel
AN
Submission Type