FDA 510(k)

CHEMONUCLEOLYSIS/DISCOGRAPHY TRAY

K-Number: K840334 · 1984-04-13

Decision Date1984-04-13

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

CHEMONUCLEOLYSIS/DISCOGRAPHY 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 1984-04-13 under 510(k) number K840334. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHEMONUCLEOLYSIS/DISCOGRAPHY TRAY?

CHEMONUCLEOLYSIS/DISCOGRAPHY TRAY is a medical device that received FDA 510(k) clearance on 1984-04-13. The listed applicant is Applied Medical Devices, Inc.. The 510(k) number is K840334.

When did CHEMONUCLEOLYSIS/DISCOGRAPHY TRAY receive FDA 510(k) clearance?

CHEMONUCLEOLYSIS/DISCOGRAPHY TRAY received FDA 510(k) clearance on 1984-04-13, under 510(k) number K840334.

Who is the listed applicant for CHEMONUCLEOLYSIS/DISCOGRAPHY 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 CHEMONUCLEOLYSIS/DISCOGRAPHY TRAY?

The FDA product code for CHEMONUCLEOLYSIS/DISCOGRAPHY TRAY is FMI.

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Other records listing Applied Medical Devices, Inc. as applicant

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Related Devices (Code: FMI)

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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.