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FDA 510(k)

DATABASE MANAGEMENT & REPORTING SYSTEM

K-Number: K792677 · 1980-01-04

ApplicantHoneywell, Inc.
Decision Date1980-01-04
Product CodeDQK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DATABASE MANAGEMENT & REPORTING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Honeywell, Inc.. It received FDA 510(k) clearance on 1980-01-04 under 510(k) number K792677. The device is classified under product code DQK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DATABASE MANAGEMENT & REPORTING SYSTEM?

DATABASE MANAGEMENT & REPORTING SYSTEM is a medical device that received FDA 510(k) clearance on 1980-01-04. The listed applicant is Honeywell, Inc.. The 510(k) number is K792677.

When did DATABASE MANAGEMENT & REPORTING SYSTEM receive FDA 510(k) clearance?

DATABASE MANAGEMENT & REPORTING SYSTEM received FDA 510(k) clearance on 1980-01-04, under 510(k) number K792677.

Who is the listed applicant for DATABASE MANAGEMENT & REPORTING SYSTEM?

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 DATABASE MANAGEMENT & REPORTING SYSTEM?

The FDA product code for DATABASE MANAGEMENT & REPORTING SYSTEM is DQK.

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Other records listing Honeywell, Inc. as applicant

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Related Devices (Code: DQK)

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.

K261729EnSite™ X EP SystemAbbott MedicalK262005Affera Integrated Mapping SystemMedtronic, Inc.K253692AVVIGO™+ Multi-Modality Guidance SystemBoston ScientificK253576CorVista System® with PCWP Add-OnAnalytics For Life, Inc.K262006EnSite™ X EP SystemAbbott MedicalK252978ScioCardio ECG Analysis PlatformSynergen Technology Labs, LLC

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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