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FDA 510(k)

SAFESET RESERVOIR

K-Number: K932188 · 1993-10-25

ApplicantAbbott Laboratories
Decision Date1993-10-25
Product CodeKRA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SAFESET RESERVOIR is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1993-10-25 under 510(k) number K932188. The device is classified under product code KRA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAFESET RESERVOIR?

SAFESET RESERVOIR is a medical device that received FDA 510(k) clearance on 1993-10-25. The listed applicant is Abbott Laboratories. The 510(k) number is K932188.

When did SAFESET RESERVOIR receive FDA 510(k) clearance?

SAFESET RESERVOIR received FDA 510(k) clearance on 1993-10-25, under 510(k) number K932188.

Who is the listed applicant for SAFESET RESERVOIR?

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

What is the FDA product code for SAFESET RESERVOIR?

The FDA product code for SAFESET RESERVOIR is KRA.

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Other records listing Abbott Laboratories as applicant

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Related Devices (Code: KRA)

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.

K253509TriSalus TriNav Advance Infusion SystemTrisalus Life SciencesK254051Extroducer Infusion Catheter SystemSmartWise Sweden ABK261610Verge™ MicrocatheterInstylla, Inc.K260771TruSelect™ 2.6 MicrocatheterBoston Scientific CorporationK250794InVera Infusion DeviceInvera MedicalK243534Micro CatheterSuzhou Zenith Vascular SciTech Limited

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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