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FDA 510(k)

DYNACOR URETHRAL CATHETER TRAY

K-Number: K821970 · 1982-07-21

Decision Date1982-07-21
Product CodeKOD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DYNACOR URETHRAL CATHETER TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 1982-07-21 under 510(k) number K821970. The device is classified under product code KOD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DYNACOR URETHRAL CATHETER TRAY?

DYNACOR URETHRAL CATHETER TRAY is a medical device that received FDA 510(k) clearance on 1982-07-21. The listed applicant is Medline Industries, Inc.. The 510(k) number is K821970.

When did DYNACOR URETHRAL CATHETER TRAY receive FDA 510(k) clearance?

DYNACOR URETHRAL CATHETER TRAY received FDA 510(k) clearance on 1982-07-21, under 510(k) number K821970.

Who is the listed applicant for DYNACOR URETHRAL CATHETER TRAY?

The FDA 510(k) record lists Medline Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DYNACOR URETHRAL CATHETER TRAY?

The FDA product code for DYNACOR URETHRAL CATHETER TRAY is KOD.

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 Medline Industries, 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.

View all 223 devices →

Related Devices (Code: KOD)

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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