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FDA 510(k)

EZ SPRAY

K-Number: K972397 · 1997-09-23

ApplicantIntertex Research, Inc.
Decision Date1997-09-23
Product CodeCCQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

EZ SPRAY is the device name listed in this FDA 510(k) record. The listed applicant is Intertex Research, Inc.. It received FDA 510(k) clearance on 1997-09-23 under 510(k) number K972397. 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 EZ SPRAY?

EZ SPRAY is a medical device that received FDA 510(k) clearance on 1997-09-23. The listed applicant is Intertex Research, Inc.. The 510(k) number is K972397.

When did EZ SPRAY receive FDA 510(k) clearance?

EZ SPRAY received FDA 510(k) clearance on 1997-09-23, under 510(k) number K972397.

Who is the listed applicant for EZ SPRAY?

The FDA 510(k) record lists Intertex Research, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EZ SPRAY?

The FDA product code for EZ SPRAY 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.

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.K900576MODIFIED AEROCHAMBER WITH MASKMonaghan Medical Corp.

Official Source

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

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