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FDA 510(k)

RHINOTEST MP

K-Number: K853024 · 1985-09-27

ApplicantIntertronic, Inc.
Decision Date1985-09-27
Product CodeBXQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RHINOTEST MP is the device name listed in this FDA 510(k) record. The listed applicant is Intertronic, Inc.. It received FDA 510(k) clearance on 1985-09-27 under 510(k) number K853024. The device is classified under product code BXQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RHINOTEST MP?

RHINOTEST MP is a medical device that received FDA 510(k) clearance on 1985-09-27. The listed applicant is Intertronic, Inc.. The 510(k) number is K853024.

When did RHINOTEST MP receive FDA 510(k) clearance?

RHINOTEST MP received FDA 510(k) clearance on 1985-09-27, under 510(k) number K853024.

Who is the listed applicant for RHINOTEST MP?

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

What is the FDA product code for RHINOTEST MP?

The FDA product code for RHINOTEST MP is BXQ.

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Related Devices (Code: BXQ)

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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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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