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FDA 510(k)

MODIFIED MODELS 9500,9550,9200,8200,HEART RATE MON

K-Number: K902785 · 1990-07-13

ApplicantAequitron Medical, Inc.
Decision Date1990-07-13
Product CodeBZQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODIFIED MODELS 9500,9550,9200,8200,HEART RATE MON is the device name listed in this FDA 510(k) record. The listed applicant is Aequitron Medical, Inc.. It received FDA 510(k) clearance on 1990-07-13 under 510(k) number K902785. The device is classified under product code BZQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED MODELS 9500,9550,9200,8200,HEART RATE MON?

MODIFIED MODELS 9500,9550,9200,8200,HEART RATE MON is a medical device that received FDA 510(k) clearance on 1990-07-13. The listed applicant is Aequitron Medical, Inc.. The 510(k) number is K902785.

When did MODIFIED MODELS 9500,9550,9200,8200,HEART RATE MON receive FDA 510(k) clearance?

MODIFIED MODELS 9500,9550,9200,8200,HEART RATE MON received FDA 510(k) clearance on 1990-07-13, under 510(k) number K902785.

Who is the listed applicant for MODIFIED MODELS 9500,9550,9200,8200,HEART RATE MON?

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

What is the FDA product code for MODIFIED MODELS 9500,9550,9200,8200,HEART RATE MON?

The FDA product code for MODIFIED MODELS 9500,9550,9200,8200,HEART RATE MON is BZQ.

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Other records listing Aequitron Medical, Inc. as applicant

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Related Devices (Code: BZQ)

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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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