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FDA 510(k)

MAXIMA FILTERED HARDSHELL RESERVOIR

K-Number: K932254 · 1993-08-03

Decision Date1993-08-03
Product CodeDTB
Advisory CommitteeCV
DecisionUnknown

Device Summary

MAXIMA FILTERED HARDSHELL RESERVOIR is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1993-08-03 under 510(k) number K932254. The device is classified under product code DTB. It was reviewed by the CV advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the MAXIMA FILTERED HARDSHELL RESERVOIR?

MAXIMA FILTERED HARDSHELL RESERVOIR is a medical device that received FDA 510(k) clearance on 1993-08-03. The listed applicant is Medtronic Vascular. The 510(k) number is K932254.

When did MAXIMA FILTERED HARDSHELL RESERVOIR receive FDA 510(k) clearance?

MAXIMA FILTERED HARDSHELL RESERVOIR received FDA 510(k) clearance on 1993-08-03, under 510(k) number K932254.

Who is the listed applicant for MAXIMA FILTERED HARDSHELL RESERVOIR?

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

What is the FDA product code for MAXIMA FILTERED HARDSHELL RESERVOIR?

The FDA product code for MAXIMA FILTERED HARDSHELL RESERVOIR is DTB.

Related Clinical Trials

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.

Other records listing Medtronic Vascular 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.

View all 474 devices →

Related Devices (Code: DTB)

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.

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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