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FDA 510(k)

MEDIPART CORRUGATED POLYETHYLENE & E.V.A. TUBING

K-Number: K853569 · 1985-11-07

Decision Date1985-11-07
Product CodeBYX
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MEDIPART CORRUGATED POLYETHYLENE & E.V.A. TUBING is the device name listed in this FDA 510(k) record. The listed applicant is Medipart Jerry Alexander. It received FDA 510(k) clearance on 1985-11-07 under 510(k) number K853569. The device is classified under product code BYX. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 49 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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