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FDA 510(k)

MODEL 6213 REMOTE ALARM

K-Number: K914424 · 1992-09-10

ApplicantAequitron Medical, Inc.
Decision Date1992-09-10
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODEL 6213 REMOTE ALARM 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 1992-09-10 under 510(k) number K914424. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 6213 REMOTE ALARM?

MODEL 6213 REMOTE ALARM is a medical device that received FDA 510(k) clearance on 1992-09-10. The listed applicant is Aequitron Medical, Inc.. The 510(k) number is K914424.

When did MODEL 6213 REMOTE ALARM receive FDA 510(k) clearance?

MODEL 6213 REMOTE ALARM received FDA 510(k) clearance on 1992-09-10, under 510(k) number K914424.

Who is the listed applicant for MODEL 6213 REMOTE ALARM?

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 MODEL 6213 REMOTE ALARM?

The FDA product code for MODEL 6213 REMOTE ALARM is CBK.

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Related Devices (Code: CBK)

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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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