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FDA 510(k)

OIC MODEL J4 TMJ CPM

K-Number: K921348 · 1992-08-05

ApplicantLm Product Design, Inc.
Decision Date1992-08-05
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

OIC MODEL J4 TMJ CPM is the device name listed in this FDA 510(k) record. The listed applicant is Lm Product Design, Inc.. It received FDA 510(k) clearance on 1992-08-05 under 510(k) number K921348. The device is classified under product code BXB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OIC MODEL J4 TMJ CPM?

OIC MODEL J4 TMJ CPM is a medical device that received FDA 510(k) clearance on 1992-08-05. The listed applicant is Lm Product Design, Inc.. The 510(k) number is K921348.

When did OIC MODEL J4 TMJ CPM receive FDA 510(k) clearance?

OIC MODEL J4 TMJ CPM received FDA 510(k) clearance on 1992-08-05, under 510(k) number K921348.

Who is the listed applicant for OIC MODEL J4 TMJ CPM?

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

What is the FDA product code for OIC MODEL J4 TMJ CPM?

The FDA product code for OIC MODEL J4 TMJ CPM is BXB.

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Related Devices (Code: BXB)

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.

K072887G-TRAINER MEDICALAlter-G, Inc.K003272FLO-BOOTDiscovery Group, LLCK952975ANKLE CALF EXERCISER PHLEBOPUMPPrevent Products, Inc.K953456E-Z FLEXFluid Motion Biotechnologies, Inc.K955105BTE CPM-10Baltimore Therapeutic Equipment Co.K955106BTE CPM-20Baltimore Therapeutic Equipment Co.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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