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FDA 510(k)

SMITH AND DAVIS PRESSURE THERAPY SYSTEM

K-Number: K913654 · 1991-11-22

ApplicantSmith & Davis Mfg. Co.
Decision Date1991-11-22
Product CodeINX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SMITH AND DAVIS PRESSURE THERAPY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Davis Mfg. Co.. It received FDA 510(k) clearance on 1991-11-22 under 510(k) number K913654. The device is classified under product code INX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMITH AND DAVIS PRESSURE THERAPY SYSTEM?

SMITH AND DAVIS PRESSURE THERAPY SYSTEM is a medical device that received FDA 510(k) clearance on 1991-11-22. The listed applicant is Smith & Davis Mfg. Co.. The 510(k) number is K913654.

When did SMITH AND DAVIS PRESSURE THERAPY SYSTEM receive FDA 510(k) clearance?

SMITH AND DAVIS PRESSURE THERAPY SYSTEM received FDA 510(k) clearance on 1991-11-22, under 510(k) number K913654.

Who is the listed applicant for SMITH AND DAVIS PRESSURE THERAPY SYSTEM?

The FDA 510(k) record lists Smith & Davis Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SMITH AND DAVIS PRESSURE THERAPY SYSTEM?

The FDA product code for SMITH AND DAVIS PRESSURE THERAPY SYSTEM is INX.

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Related Devices (Code: INX)

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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.

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