MEDIPART CORRUGATED POLYETHYLENE & E.V.A. TUBING
K-Number: K853569 · 1985-11-07
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Device Summary
Frequently Asked Questions
What is the MEDIPART CORRUGATED POLYETHYLENE & E.V.A. TUBING?
MEDIPART CORRUGATED POLYETHYLENE & E.V.A. TUBING is a medical device that received FDA 510(k) clearance on 1985-11-07. The listed applicant is Medipart Jerry Alexander. The 510(k) number is K853569.
When did MEDIPART CORRUGATED POLYETHYLENE & E.V.A. TUBING receive FDA 510(k) clearance?
MEDIPART CORRUGATED POLYETHYLENE & E.V.A. TUBING received FDA 510(k) clearance on 1985-11-07, under 510(k) number K853569.
Who is the listed applicant for MEDIPART CORRUGATED POLYETHYLENE & E.V.A. TUBING?
The FDA 510(k) record lists Medipart Jerry Alexander as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MEDIPART CORRUGATED POLYETHYLENE & E.V.A. TUBING?
The FDA product code for MEDIPART CORRUGATED POLYETHYLENE & E.V.A. TUBING is BYX.
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 Medipart Jerry Alexander 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: BYX)
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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