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FDA 510(k)

TRANSTHORACIC/TRANSABDOMINAL-TRAY

K-Number: K833720 · 1984-05-30

ApplicantApplied Medical Devices, Inc.
Decision Date1984-05-30
Product CodeGDM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TRANSTHORACIC/TRANSABDOMINAL-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 1984-05-30 under 510(k) number K833720. The device is classified under product code GDM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRANSTHORACIC/TRANSABDOMINAL-TRAY?

TRANSTHORACIC/TRANSABDOMINAL-TRAY is a medical device that received FDA 510(k) clearance on 1984-05-30. The listed applicant is Applied Medical Devices, Inc.. The 510(k) number is K833720.

When did TRANSTHORACIC/TRANSABDOMINAL-TRAY receive FDA 510(k) clearance?

TRANSTHORACIC/TRANSABDOMINAL-TRAY received FDA 510(k) clearance on 1984-05-30, under 510(k) number K833720.

Who is the listed applicant for TRANSTHORACIC/TRANSABDOMINAL-TRAY?

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

What is the FDA product code for TRANSTHORACIC/TRANSABDOMINAL-TRAY?

The FDA product code for TRANSTHORACIC/TRANSABDOMINAL-TRAY is GDM.

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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 CHOLANK843884GENERAL UTILITY TRAY SYSTEMK840904ACCU-CULT FECAL OCCULT BLOOD TESTK842591ULTRASOUND PROBE COVERS-STERILEK840334CHEMONUCLEOLYSIS/DISCOGRAPHY TRAY

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Related Devices (Code: GDM)

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.

K071732MARROWMINERStemcor Systems, Inc.K971114BIOACCESS MARROW HARVEST SYSTEMBioaccess, Inc.K953082ILIAC CREST BONE MARROW ASPIRATION NEEDLEBaxter Healthcare CorpK953064BIOACCESS MARROW HARVEST SYSTEMBioaccess, Inc.K936207ENDO-NEEDLE INSTRUMENTGerard Medical, Inc.K930160ILLINOIS STERNAL/ILIAC ASPIRATION NEEDLESymbiosis Corp.

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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