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FDA 510(k)

VITALERT 2000 VITAL SIGNS MONITOR

K-Number: K882031 · 1988-07-28

ApplicantDraeger Medical, Inc.
Decision Date1988-07-28
Product CodeDXO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VITALERT 2000 VITAL SIGNS MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Draeger Medical, Inc.. It received FDA 510(k) clearance on 1988-07-28 under 510(k) number K882031. The device is classified under product code DXO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITALERT 2000 VITAL SIGNS MONITOR?

VITALERT 2000 VITAL SIGNS MONITOR is a medical device that received FDA 510(k) clearance on 1988-07-28. The listed applicant is Draeger Medical, Inc.. The 510(k) number is K882031.

When did VITALERT 2000 VITAL SIGNS MONITOR receive FDA 510(k) clearance?

VITALERT 2000 VITAL SIGNS MONITOR received FDA 510(k) clearance on 1988-07-28, under 510(k) number K882031.

Who is the listed applicant for VITALERT 2000 VITAL SIGNS MONITOR?

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

What is the FDA product code for VITALERT 2000 VITAL SIGNS MONITOR?

The FDA product code for VITALERT 2000 VITAL SIGNS MONITOR is DXO.

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Other records listing Draeger Medical, Inc. 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.

K042607PRIMUS USK042419FABIUS GS/FABIUS TIRO ANESTHESIA SYSTEMK042276D-VAPORK042086FABIUS GS ANESTHESIA SYSTEM; FABIUS TIRO ANESTHESIA SYSTEMK041622MODIFICATION TO FABIUS GS ANESTHESIA SYSTEM; FABIUS TIRO ANESTHESIA SYSTEMK040847MODIFICATION TO VAMOS ANESTHETIC GAS MONITOR

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Related Devices (Code: DXO)

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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