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FDA 510(k)

TMJ CANNULA SET

K-Number: K871648 · 1987-06-08

ApplicantAspen Laboratories, Inc.
Decision Date1987-06-08
Product CodeDZI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TMJ CANNULA SET is the device name listed in this FDA 510(k) record. The listed applicant is Aspen Laboratories, Inc.. It received FDA 510(k) clearance on 1987-06-08 under 510(k) number K871648. The device is classified under product code DZI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TMJ CANNULA SET?

TMJ CANNULA SET is a medical device that received FDA 510(k) clearance on 1987-06-08. The listed applicant is Aspen Laboratories, Inc.. The 510(k) number is K871648.

When did TMJ CANNULA SET receive FDA 510(k) clearance?

TMJ CANNULA SET received FDA 510(k) clearance on 1987-06-08, under 510(k) number K871648.

Who is the listed applicant for TMJ CANNULA SET?

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

What is the FDA product code for TMJ CANNULA SET?

The FDA product code for TMJ CANNULA SET is DZI.

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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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