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FDA 510(k)

PERCUTANEOUS ASPIRATION BIOPSY TRAY

K-Number: K843885 · 1984-12-19

ApplicantApplied Medical Devices, Inc.
Decision Date1984-12-19
Product Code
DecisionSubstantially Equivalent

Device Summary

PERCUTANEOUS ASPIRATION BIOPSY TRAY 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 1984-12-19 under 510(k) number K843885. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERCUTANEOUS ASPIRATION BIOPSY TRAY?

PERCUTANEOUS ASPIRATION BIOPSY TRAY is a medical device that received FDA 510(k) clearance on 1984-12-19. The listed applicant is Applied Medical Devices, Inc.. The 510(k) number is K843885.

When did PERCUTANEOUS ASPIRATION BIOPSY TRAY receive FDA 510(k) clearance?

PERCUTANEOUS ASPIRATION BIOPSY TRAY received FDA 510(k) clearance on 1984-12-19, under 510(k) number K843885.

Who is the listed applicant for PERCUTANEOUS ASPIRATION BIOPSY TRAY?

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.

K843884GENERAL UTILITY TRAY SYSTEMK843883STERILE 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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