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FDA 510(k)

GENERAL UTILITY TRAY SYSTEM

K-Number: K843884 · 1984-12-13

ApplicantApplied Medical Devices, Inc.
Decision Date1984-12-13
Product Code
DecisionSubstantially Equivalent

Device Summary

GENERAL UTILITY TRAY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical Devices, Inc.. It received FDA 510(k) clearance on 1984-12-13 under 510(k) number K843884. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GENERAL UTILITY TRAY SYSTEM?

GENERAL UTILITY TRAY SYSTEM is a medical device that received FDA 510(k) clearance on 1984-12-13. The listed applicant is Applied Medical Devices, Inc.. The 510(k) number is K843884.

When did GENERAL UTILITY TRAY SYSTEM receive FDA 510(k) clearance?

GENERAL UTILITY TRAY SYSTEM received FDA 510(k) clearance on 1984-12-13, under 510(k) number K843884.

Who is the listed applicant for GENERAL UTILITY TRAY SYSTEM?

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

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Other records listing Applied Medical Devices, 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.

K843885PERCUTANEOUS ASPIRATION BIOPSY TRAYK843883STERILE PERCUTANEOUS TRANSHEPATIC CHOLANK840904ACCU-CULT FECAL OCCULT BLOOD TESTK842591ULTRASOUND PROBE COVERS-STERILEK833720TRANSTHORACIC/TRANSABDOMINAL-TRAYK840334CHEMONUCLEOLYSIS/DISCOGRAPHY TRAY

View all 11 devices →

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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