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FDA 510(k)

WORK SIMULATOR

K-Number: K800007 · 1980-01-21

ApplicantBaltimore Therapeutic Equipment Co.
Decision Date1980-01-21
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

WORK SIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Baltimore Therapeutic Equipment Co.. It received FDA 510(k) clearance on 1980-01-21 under 510(k) number K800007. 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 WORK SIMULATOR?

WORK SIMULATOR is a medical device that received FDA 510(k) clearance on 1980-01-21. The listed applicant is Baltimore Therapeutic Equipment Co.. The 510(k) number is K800007.

When did WORK SIMULATOR receive FDA 510(k) clearance?

WORK SIMULATOR received FDA 510(k) clearance on 1980-01-21, under 510(k) number K800007.

Who is the listed applicant for WORK SIMULATOR?

The FDA 510(k) record lists Baltimore Therapeutic Equipment Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WORK SIMULATOR?

The FDA product code for WORK SIMULATOR is BXB.

Related Clinical Trials

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.

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Other records listing Baltimore Therapeutic Equipment Co. as applicant

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.

K955106BTE CPM-20K955105BTE CPM-10K925225THE BTE VECTOR; ANALYSIS SYSTEM FOR THE LOW BACKK933611THE BTE WS30K924414THE BTE DYNAMIC LIFTK895881MOTIONSPECT

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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

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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