SUPERPLAST Double-Occluder, SUPERPLAST Vascular Probe
K-Number: K220981 · 2023-04-20
Device Summary
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. The listed applicant is Fehling Surgical Instruments, Inc.. The 510(k) number is K220981.
When did SUPERPLAST Double-Occluder, SUPERPLAST Vascular Probe receive FDA 510(k) clearance?
SUPERPLAST Double-Occluder, SUPERPLAST Vascular Probe received FDA 510(k) clearance on 2023-04-20, under 510(k) number K220981.
Who is the listed applicant for SUPERPLAST Double-Occluder, SUPERPLAST Vascular Probe?
The FDA 510(k) record lists Fehling Surgical Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
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.
Related Devices (Code: DWP)
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
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