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FDA 510(k)

SUPERPLAST Double-Occluder, SUPERPLAST Vascular Probe

K-Number: K220981 · 2023-04-20

ApplicantFehling Surgical Instruments, Inc.
Decision Date2023-04-20
Product CodeDWP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SUPERPLAST Double-Occluder, SUPERPLAST Vascular Probe is a medical device manufactured by Fehling Surgical Instruments, Inc.. It received FDA 510(k) clearance on 2023-04-20 under approval number K220981. The device is classified under product code DWP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUPERPLAST Double-Occluder, SUPERPLAST Vascular Probe?

SUPERPLAST Double-Occluder, SUPERPLAST Vascular Probe is a medical device that received FDA 510(k) clearance on 2023-04-20. It is manufactured by Fehling Surgical Instruments, Inc.. The 510(k) number is K220981.

When was SUPERPLAST Double-Occluder, SUPERPLAST Vascular Probe approved by the FDA?

SUPERPLAST Double-Occluder, SUPERPLAST Vascular Probe received FDA 510(k) clearance on 2023-04-20, under approval number K220981.

What company makes SUPERPLAST Double-Occluder, SUPERPLAST Vascular Probe?

SUPERPLAST Double-Occluder, SUPERPLAST Vascular Probe is manufactured by Fehling Surgical Instruments, Inc..

What is the FDA product code for SUPERPLAST Double-Occluder, SUPERPLAST Vascular Probe?

The FDA product code for SUPERPLAST Double-Occluder, SUPERPLAST Vascular Probe is DWP.

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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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