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FDA 510(k)

ALLERGEN CONTROL INHALENT

K-Number: K832218 · 1983-09-20

ApplicantVentrex Laboratories, Inc.
Decision Date1983-09-20
Product CodeDGC
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

ALLERGEN CONTROL INHALENT is the device name listed in this FDA 510(k) record. The listed applicant is Ventrex Laboratories, Inc.. It received FDA 510(k) clearance on 1983-09-20 under 510(k) number K832218. The device is classified under product code DGC. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALLERGEN CONTROL INHALENT?

ALLERGEN CONTROL INHALENT is a medical device that received FDA 510(k) clearance on 1983-09-20. The listed applicant is Ventrex Laboratories, Inc.. The 510(k) number is K832218.

When did ALLERGEN CONTROL INHALENT receive FDA 510(k) clearance?

ALLERGEN CONTROL INHALENT received FDA 510(k) clearance on 1983-09-20, under 510(k) number K832218.

Who is the listed applicant for ALLERGEN CONTROL INHALENT?

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

What is the FDA product code for ALLERGEN CONTROL INHALENT?

The FDA product code for ALLERGEN CONTROL INHALENT is DGC.

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Other records listing Ventrex Laboratories, 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.

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Related Devices (Code: DGC)

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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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