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FDA 510(k)

STAND AID

K-Number: K872934 · 1987-11-23

ApplicantStand Aid of Iowa, Inc.
Decision Date1987-11-23
Product CodeIPL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

STAND AID is the device name listed in this FDA 510(k) record. The listed applicant is Stand Aid of Iowa, Inc.. It received FDA 510(k) clearance on 1987-11-23 under 510(k) number K872934. The device is classified under product code IPL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STAND AID?

STAND AID is a medical device that received FDA 510(k) clearance on 1987-11-23. The listed applicant is Stand Aid of Iowa, Inc.. The 510(k) number is K872934.

When did STAND AID receive FDA 510(k) clearance?

STAND AID received FDA 510(k) clearance on 1987-11-23, under 510(k) number K872934.

Who is the listed applicant for STAND AID?

The FDA 510(k) record lists Stand Aid of Iowa, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STAND AID?

The FDA product code for STAND AID is IPL.

Related Clinical Trials

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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Other records listing Stand Aid of Iowa, Inc. 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.

K970164ROLL AID

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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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