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FDA 510(k)

LOCKJAW 15 MINUTE INTERMAXILLARY FIXATION SYSTEM,MODEL LJ100-00

K-Number: K990212 · 1999-09-14

ApplicantDoctor'S Research Group, Inc.
Decision Date1999-09-14
Product CodeDYX
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LOCKJAW 15 MINUTE INTERMAXILLARY FIXATION SYSTEM,MODEL LJ100-00 is the device name listed in this FDA 510(k) record. The listed applicant is Doctor'S Research Group, Inc.. It received FDA 510(k) clearance on 1999-09-14 under 510(k) number K990212. The device is classified under product code DYX. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LOCKJAW 15 MINUTE INTERMAXILLARY FIXATION SYSTEM,MODEL LJ100-00?

LOCKJAW 15 MINUTE INTERMAXILLARY FIXATION SYSTEM,MODEL LJ100-00 is a medical device that received FDA 510(k) clearance on 1999-09-14. The listed applicant is Doctor'S Research Group, Inc.. The 510(k) number is K990212.

When did LOCKJAW 15 MINUTE INTERMAXILLARY FIXATION SYSTEM,MODEL LJ100-00 receive FDA 510(k) clearance?

LOCKJAW 15 MINUTE INTERMAXILLARY FIXATION SYSTEM,MODEL LJ100-00 received FDA 510(k) clearance on 1999-09-14, under 510(k) number K990212.

Who is the listed applicant for LOCKJAW 15 MINUTE INTERMAXILLARY FIXATION SYSTEM,MODEL LJ100-00?

The FDA 510(k) record lists Doctor'S Research Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LOCKJAW 15 MINUTE INTERMAXILLARY FIXATION SYSTEM,MODEL LJ100-00?

The FDA product code for LOCKJAW 15 MINUTE INTERMAXILLARY FIXATION SYSTEM,MODEL LJ100-00 is DYX.

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Other records listing Doctor'S Research Group, Inc. as applicant

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Related Devices (Code: DYX)

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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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