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FDA 510(k)

ALTAIR

K-Number: K912728 · 1992-02-27

ApplicantDiagnostic Medical Instruments
Decision Date1992-02-27
Product CodeDQK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ALTAIR is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Medical Instruments. It received FDA 510(k) clearance on 1992-02-27 under 510(k) number K912728. 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 ALTAIR?

ALTAIR is a medical device that received FDA 510(k) clearance on 1992-02-27. The listed applicant is Diagnostic Medical Instruments. The 510(k) number is K912728.

When did ALTAIR receive FDA 510(k) clearance?

ALTAIR received FDA 510(k) clearance on 1992-02-27, under 510(k) number K912728.

Who is the listed applicant for ALTAIR?

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

What is the FDA product code for ALTAIR?

The FDA product code for ALTAIR is DQK.

Related Clinical Trials

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Other records listing Diagnostic Medical Instruments as applicant

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.

K894285DMI PC HOLTER SCANNERK871045DMI AMBULATORY HOLTER MONITORK830489RECORDER DMIK830407ECLIPSE

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

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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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