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FDA 510(k)

PRECONNECTED URETHRAL CATHETER TRAY

K-Number: K850152 · 1985-03-12

ApplicantInmed Corp.
Decision Date1985-03-12
Product Code
DecisionSubstantially Equivalent

Device Summary

PRECONNECTED URETHRAL CATHETER TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Inmed Corp.. It received FDA 510(k) clearance on 1985-03-12 under 510(k) number K850152. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRECONNECTED URETHRAL CATHETER TRAY?

PRECONNECTED URETHRAL CATHETER TRAY is a medical device that received FDA 510(k) clearance on 1985-03-12. The listed applicant is Inmed Corp.. The 510(k) number is K850152.

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

PRECONNECTED URETHRAL CATHETER TRAY received FDA 510(k) clearance on 1985-03-12, under 510(k) number K850152.

Who is the listed applicant for PRECONNECTED URETHRAL CATHETER TRAY?

The FDA 510(k) record lists Inmed Corp. as the applicant. This does not by itself establish the device manufacturer.

Related Clinical Trials

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Other records listing Inmed Corp. 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.

K862672ESOPHAGEAL STETHOSCOPE WITH THERMISTORK853162STERILE NASOPHARYNGEAL AIRWAYK850335URETEROSCOPY CATHETERK850248DISPOSABLE GUEDEL AIRWAYK844801ULTRA EXTERNAL CATHETERK842301DISPOSABLE LATEX BANDAGE

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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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