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FDA 510(k)

VITALSAT SERIES

K-Number: K011518 · 2002-11-15

ApplicantBeta Biomed Services, Inc.
Decision Date2002-11-15
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VITALSAT SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Beta Biomed Services, Inc.. It received FDA 510(k) clearance on 2002-11-15 under 510(k) number K011518. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITALSAT SERIES?

VITALSAT SERIES is a medical device that received FDA 510(k) clearance on 2002-11-15. The listed applicant is Beta Biomed Services, Inc.. The 510(k) number is K011518.

When did VITALSAT SERIES receive FDA 510(k) clearance?

VITALSAT SERIES received FDA 510(k) clearance on 2002-11-15, under 510(k) number K011518.

Who is the listed applicant for VITALSAT SERIES?

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

What is the FDA product code for VITALSAT SERIES?

The FDA product code for VITALSAT SERIES is DQA.

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Other records listing Beta Biomed Services, 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.

K003542PREAMP CABLE, MODEL B400-1011PA

Related Devices (Code: DQA)

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

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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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