LUNDERQUIST - RING PTC DRAINAGE CATHETER
K-Number: K861220 · 1986-05-19
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Device Summary
Frequently Asked Questions
What is the LUNDERQUIST - RING PTC DRAINAGE CATHETER?
LUNDERQUIST - RING PTC DRAINAGE CATHETER is a medical device that received FDA 510(k) clearance on 1986-05-19. The listed applicant is Meadox Surgimed, Inc.. The 510(k) number is K861220.
When did LUNDERQUIST - RING PTC DRAINAGE CATHETER receive FDA 510(k) clearance?
LUNDERQUIST - RING PTC DRAINAGE CATHETER received FDA 510(k) clearance on 1986-05-19, under 510(k) number K861220.
Who is the listed applicant for LUNDERQUIST - RING PTC DRAINAGE CATHETER?
The FDA 510(k) record lists Meadox Surgimed, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LUNDERQUIST - RING PTC DRAINAGE CATHETER?
The FDA product code for LUNDERQUIST - RING PTC DRAINAGE CATHETER is FGE.
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 Meadox Surgimed, Inc. 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.
Related Devices (Code: FGE)
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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