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FDA 510(k)

MAGGI SERIES ULTRA. NEEDLE, BIOPSY/CATHETER GUIDES

K-Number: K882383 · 1988-11-28

ApplicantCIVCO Medical Instruments Co., Inc.
Decision Date1988-11-28
Product CodeDWZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MAGGI SERIES ULTRA. NEEDLE, BIOPSY/CATHETER GUIDES is the device name listed in this FDA 510(k) record. The listed applicant is CIVCO Medical Instruments Co., Inc.. It received FDA 510(k) clearance on 1988-11-28 under 510(k) number K882383. The device is classified under product code DWZ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAGGI SERIES ULTRA. NEEDLE, BIOPSY/CATHETER GUIDES?

MAGGI SERIES ULTRA. NEEDLE, BIOPSY/CATHETER GUIDES is a medical device that received FDA 510(k) clearance on 1988-11-28. The listed applicant is CIVCO Medical Instruments Co., Inc.. The 510(k) number is K882383.

When did MAGGI SERIES ULTRA. NEEDLE, BIOPSY/CATHETER GUIDES receive FDA 510(k) clearance?

MAGGI SERIES ULTRA. NEEDLE, BIOPSY/CATHETER GUIDES received FDA 510(k) clearance on 1988-11-28, under 510(k) number K882383.

Who is the listed applicant for MAGGI SERIES ULTRA. NEEDLE, BIOPSY/CATHETER GUIDES?

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

What is the FDA product code for MAGGI SERIES ULTRA. NEEDLE, BIOPSY/CATHETER GUIDES?

The FDA product code for MAGGI SERIES ULTRA. NEEDLE, BIOPSY/CATHETER GUIDES is DWZ.

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Related Devices (Code: DWZ)

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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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