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FDA 510(k)

MOTIONSPECT

K-Number: K895881 · 1990-04-10

ApplicantBaltimore Therapeutic Equipment Co.
Decision Date1990-04-10
Product CodeLXW
DecisionSubstantially Equivalent

Device Summary

MOTIONSPECT 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 1990-04-10 under 510(k) number K895881. The device is classified under product code LXW. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOTIONSPECT?

MOTIONSPECT is a medical device that received FDA 510(k) clearance on 1990-04-10. The listed applicant is Baltimore Therapeutic Equipment Co.. The 510(k) number is K895881.

When did MOTIONSPECT receive FDA 510(k) clearance?

MOTIONSPECT received FDA 510(k) clearance on 1990-04-10, under 510(k) number K895881.

Who is the listed applicant for MOTIONSPECT?

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 MOTIONSPECT?

The FDA product code for MOTIONSPECT is LXW.

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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.

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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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