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FDA 510(k)

THE BTE DYNAMIC LIFT

K-Number: K924414 · 1993-02-12

ApplicantBaltimore Therapeutic Equipment Co.
Decision Date1993-02-12
Product CodeIKK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

THE BTE DYNAMIC LIFT 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 1993-02-12 under 510(k) number K924414. The device is classified under product code IKK. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE BTE DYNAMIC LIFT?

THE BTE DYNAMIC LIFT is a medical device that received FDA 510(k) clearance on 1993-02-12. The listed applicant is Baltimore Therapeutic Equipment Co.. The 510(k) number is K924414.

When did THE BTE DYNAMIC LIFT receive FDA 510(k) clearance?

THE BTE DYNAMIC LIFT received FDA 510(k) clearance on 1993-02-12, under 510(k) number K924414.

Who is the listed applicant for THE BTE DYNAMIC LIFT?

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 THE BTE DYNAMIC LIFT?

The FDA product code for THE BTE DYNAMIC LIFT is IKK.

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Other records listing Baltimore Therapeutic Equipment Co. as applicant

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Related Devices (Code: IKK)

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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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