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FDA 510(k)

MANDIBULATOR JAW POSITIONER

K-Number: K843705 · 1984-11-14

ApplicantA Company, Inc.
Decision Date1984-11-14
Product CodeDYJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MANDIBULATOR JAW POSITIONER is the device name listed in this FDA 510(k) record. The listed applicant is A Company, Inc.. It received FDA 510(k) clearance on 1984-11-14 under 510(k) number K843705. The device is classified under product code DYJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MANDIBULATOR JAW POSITIONER?

MANDIBULATOR JAW POSITIONER is a medical device that received FDA 510(k) clearance on 1984-11-14. The listed applicant is A Company, Inc.. The 510(k) number is K843705.

When did MANDIBULATOR JAW POSITIONER receive FDA 510(k) clearance?

MANDIBULATOR JAW POSITIONER received FDA 510(k) clearance on 1984-11-14, under 510(k) number K843705.

Who is the listed applicant for MANDIBULATOR JAW POSITIONER?

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

What is the FDA product code for MANDIBULATOR JAW POSITIONER?

The FDA product code for MANDIBULATOR JAW POSITIONER is DYJ.

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Other records listing A Company, Inc. as applicant

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Related Devices (Code: DYJ)

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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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