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FDA 510(k)

SERIES 3 GENERAL SUCTION SYSTEM

K-Number: K891129 · 1989-09-25

ApplicantUltravac, Inc.
Decision Date1989-09-25
Product CodeBTA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SERIES 3 GENERAL SUCTION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Ultravac, Inc.. It received FDA 510(k) clearance on 1989-09-25 under 510(k) number K891129. The device is classified under product code BTA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SERIES 3 GENERAL SUCTION SYSTEM?

SERIES 3 GENERAL SUCTION SYSTEM is a medical device that received FDA 510(k) clearance on 1989-09-25. The listed applicant is Ultravac, Inc.. The 510(k) number is K891129.

When did SERIES 3 GENERAL SUCTION SYSTEM receive FDA 510(k) clearance?

SERIES 3 GENERAL SUCTION SYSTEM received FDA 510(k) clearance on 1989-09-25, under 510(k) number K891129.

Who is the listed applicant for SERIES 3 GENERAL SUCTION SYSTEM?

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

What is the FDA product code for SERIES 3 GENERAL SUCTION SYSTEM?

The FDA product code for SERIES 3 GENERAL SUCTION SYSTEM is BTA.

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Related Devices (Code: BTA)

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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