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FDA 510(k)

AERO-VENT AEROSOL UNIT

K-Number: K865107 · 1987-10-20

ApplicantMedi Nuclear Corp., Inc.
Decision Date1987-10-20
Product CodeIYT
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AERO-VENT AEROSOL UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Medi Nuclear Corp., Inc.. It received FDA 510(k) clearance on 1987-10-20 under 510(k) number K865107. The device is classified under product code IYT. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AERO-VENT AEROSOL UNIT?

AERO-VENT AEROSOL UNIT is a medical device that received FDA 510(k) clearance on 1987-10-20. The listed applicant is Medi Nuclear Corp., Inc.. The 510(k) number is K865107.

When did AERO-VENT AEROSOL UNIT receive FDA 510(k) clearance?

AERO-VENT AEROSOL UNIT received FDA 510(k) clearance on 1987-10-20, under 510(k) number K865107.

Who is the listed applicant for AERO-VENT AEROSOL UNIT?

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

What is the FDA product code for AERO-VENT AEROSOL UNIT?

The FDA product code for AERO-VENT AEROSOL UNIT is IYT.

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Other records listing Medi Nuclear Corp., Inc. as applicant

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.

K082541HEALTHLINE MEDICATOR / REDINEB AEROSOL DRUG DELIVERY SYSTEMK080969HEALTHLINE REDI-NEB MEDICATION NEBULIZER, MODEL RN-510K080657NEB-90 LARGE VOLUME MEDICATION NEBULIZERK915075NEBULIZER (DIRECT PATIENT INTERFACE)K865093SAFE-T-SHIELD MOUTHPIECEK863996MODEL XE-103 XENON/MASTER II

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Related Devices (Code: IYT)

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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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