Synchroner TM (Proposed Tradename)

FDA 510(k) K853350 · Fisons Corp.

Substantially Equivalent

510(k) numberK853350

Submission

Device name
Synchroner TM (Proposed Tradename)
Applicant
Fisons Corp.
Bedford, MA, US
Received
August 12, 1985
Decision date
August 29, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CCQ – Nebulizer, Medicinal, Non-Ventilatory (Atomizer)
Device class
Class I (low risk)
Regulation
21 CFR 868.5640
Specialty
Anesthesiology

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Questions and answers

When was Synchroner TM (Proposed Tradename) cleared by the FDA?

Synchroner TM (Proposed Tradename) (K853350) received a 510(k) decision of Substantially Equivalent on August 29, 1985, 17 days after the submission was received.

What is the product code of K853350?

The FDA product code is CCQ – Nebulizer, Medicinal, Non-Ventilatory (Atomizer), a Class I (low risk) device regulated under 21 CFR 868.5640.