FDA 510(k)

ULTIMA BODY POSITION SENSOR

K-Number: K981969 · 1998-08-20

Decision Date1998-08-20

Product CodeLEL

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

ULTIMA BODY POSITION SENSOR is the device name listed in this FDA 510(k) record. The listed applicant is Braebon Medical Corp.. It received FDA 510(k) clearance on 1998-08-20 under 510(k) number K981969. The device is classified under product code LEL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTIMA BODY POSITION SENSOR?

ULTIMA BODY POSITION SENSOR is a medical device that received FDA 510(k) clearance on 1998-08-20. The listed applicant is Braebon Medical Corp.. The 510(k) number is K981969.

When did ULTIMA BODY POSITION SENSOR receive FDA 510(k) clearance?

ULTIMA BODY POSITION SENSOR received FDA 510(k) clearance on 1998-08-20, under 510(k) number K981969.

Who is the listed applicant for ULTIMA BODY POSITION SENSOR?

The FDA 510(k) record lists Braebon Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ULTIMA BODY POSITION SENSOR?

The FDA product code for ULTIMA BODY POSITION SENSOR is LEL.

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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.