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FDA 510(k)

AMBUL. PH & MOTILITY RECORDER FOR MEASURE OF PARA.

K-Number: K880581 · 1988-08-11

ApplicantSynectics-Dantec
Decision Date1988-08-11
Product CodeFFX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

AMBUL. PH & MOTILITY RECORDER FOR MEASURE OF PARA. is the device name listed in this FDA 510(k) record. The listed applicant is Synectics-Dantec. It received FDA 510(k) clearance on 1988-08-11 under 510(k) number K880581. The device is classified under product code FFX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMBUL. PH & MOTILITY RECORDER FOR MEASURE OF PARA.?

AMBUL. PH & MOTILITY RECORDER FOR MEASURE OF PARA. is a medical device that received FDA 510(k) clearance on 1988-08-11. The listed applicant is Synectics-Dantec. The 510(k) number is K880581.

When did AMBUL. PH & MOTILITY RECORDER FOR MEASURE OF PARA. receive FDA 510(k) clearance?

AMBUL. PH & MOTILITY RECORDER FOR MEASURE OF PARA. received FDA 510(k) clearance on 1988-08-11, under 510(k) number K880581.

Who is the listed applicant for AMBUL. PH & MOTILITY RECORDER FOR MEASURE OF PARA.?

The FDA 510(k) record lists Synectics-Dantec as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AMBUL. PH & MOTILITY RECORDER FOR MEASURE OF PARA.?

The FDA product code for AMBUL. PH & MOTILITY RECORDER FOR MEASURE OF PARA. is FFX.

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Other records listing Synectics-Dantec as applicant

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Related Devices (Code: FFX)

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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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