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FDA 510(k)

CEN STA MON AC/DC ALARM CENTRAL ACCES ALARM RECOR

K-Number: K863100 · 1987-02-03

ApplicantHoneywell, Inc.
Decision Date1987-02-03
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CEN STA MON AC/DC ALARM CENTRAL ACCES ALARM RECOR is the device name listed in this FDA 510(k) record. The listed applicant is Honeywell, Inc.. It received FDA 510(k) clearance on 1987-02-03 under 510(k) number K863100. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CEN STA MON AC/DC ALARM CENTRAL ACCES ALARM RECOR?

CEN STA MON AC/DC ALARM CENTRAL ACCES ALARM RECOR is a medical device that received FDA 510(k) clearance on 1987-02-03. The listed applicant is Honeywell, Inc.. The 510(k) number is K863100.

When did CEN STA MON AC/DC ALARM CENTRAL ACCES ALARM RECOR receive FDA 510(k) clearance?

CEN STA MON AC/DC ALARM CENTRAL ACCES ALARM RECOR received FDA 510(k) clearance on 1987-02-03, under 510(k) number K863100.

Who is the listed applicant for CEN STA MON AC/DC ALARM CENTRAL ACCES ALARM RECOR?

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

What is the FDA product code for CEN STA MON AC/DC ALARM CENTRAL ACCES ALARM RECOR?

The FDA product code for CEN STA MON AC/DC ALARM CENTRAL ACCES ALARM RECOR is DPS.

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Other records listing Honeywell, Inc. as applicant

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Related Devices (Code: DPS)

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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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