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FDA 510(k)

MONITORING SYSTEM, MODEL ARGUS PB-2200

K-Number: K033738 · 2004-08-24

ApplicantSchiller AG
Decision Date2004-08-24
Product CodeDSK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MONITORING SYSTEM, MODEL ARGUS PB-2200 is the device name listed in this FDA 510(k) record. The listed applicant is Schiller AG. It received FDA 510(k) clearance on 2004-08-24 under 510(k) number K033738. The device is classified under product code DSK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MONITORING SYSTEM, MODEL ARGUS PB-2200?

MONITORING SYSTEM, MODEL ARGUS PB-2200 is a medical device that received FDA 510(k) clearance on 2004-08-24. The listed applicant is Schiller AG. The 510(k) number is K033738.

When did MONITORING SYSTEM, MODEL ARGUS PB-2200 receive FDA 510(k) clearance?

MONITORING SYSTEM, MODEL ARGUS PB-2200 received FDA 510(k) clearance on 2004-08-24, under 510(k) number K033738.

Who is the listed applicant for MONITORING SYSTEM, MODEL ARGUS PB-2200?

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

What is the FDA product code for MONITORING SYSTEM, MODEL ARGUS PB-2200?

The FDA product code for MONITORING SYSTEM, MODEL ARGUS PB-2200 is DSK.

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Other records listing Schiller AG as applicant

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Related Devices (Code: DSK)

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.

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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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