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FDA 510(k)

INTERMITTENT SIGNAL ACTUATED NEBULIZER (VISAN)

K-Number: K873477 · 1987-10-09

ApplicantVortran Medical Technology 1, Inc.
Decision Date1987-10-09
Product CodeCCQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

INTERMITTENT SIGNAL ACTUATED NEBULIZER (VISAN) is the device name listed in this FDA 510(k) record. The listed applicant is Vortran Medical Technology 1, Inc.. It received FDA 510(k) clearance on 1987-10-09 under 510(k) number K873477. The device is classified under product code CCQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERMITTENT SIGNAL ACTUATED NEBULIZER (VISAN)?

INTERMITTENT SIGNAL ACTUATED NEBULIZER (VISAN) is a medical device that received FDA 510(k) clearance on 1987-10-09. The listed applicant is Vortran Medical Technology 1, Inc.. The 510(k) number is K873477.

When did INTERMITTENT SIGNAL ACTUATED NEBULIZER (VISAN) receive FDA 510(k) clearance?

INTERMITTENT SIGNAL ACTUATED NEBULIZER (VISAN) received FDA 510(k) clearance on 1987-10-09, under 510(k) number K873477.

Who is the listed applicant for INTERMITTENT SIGNAL ACTUATED NEBULIZER (VISAN)?

The FDA 510(k) record lists Vortran Medical Technology 1, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTERMITTENT SIGNAL ACTUATED NEBULIZER (VISAN)?

The FDA product code for INTERMITTENT SIGNAL ACTUATED NEBULIZER (VISAN) is CCQ.

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Related Devices (Code: CCQ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K972397EZ SPRAYIntertex Research, Inc.K964956E-Z SPACER MASK (SMALL)Airpharma, LLCK961894MDI TUTORMdi Tutor, Inc.K961455MEDSHIELD/AEROCHAMBERDiemolding Corp.K960593SMARTMIST ASTHMA MANAGMENT SYSTEM, SMARTMIST, MODEL NUMBER SM-100/SMARTMIST SPIROMETRY AIRWAY, MODEL NUMBER SA-100Aradigm Corp.K922033SALINE SOLUTION- STERILETrinity Laboratories, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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