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FDA 510(k)

STAIR VEYOR

K-Number: K882091 · 1988-05-26

ApplicantPride Health Care, Inc.
Decision Date1988-05-26
Product CodeILK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

STAIR VEYOR is the device name listed in this FDA 510(k) record. The listed applicant is Pride Health Care, Inc.. It received FDA 510(k) clearance on 1988-05-26 under 510(k) number K882091. The device is classified under product code ILK. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STAIR VEYOR?

STAIR VEYOR is a medical device that received FDA 510(k) clearance on 1988-05-26. The listed applicant is Pride Health Care, Inc.. The 510(k) number is K882091.

When did STAIR VEYOR receive FDA 510(k) clearance?

STAIR VEYOR received FDA 510(k) clearance on 1988-05-26, under 510(k) number K882091.

Who is the listed applicant for STAIR VEYOR?

The FDA 510(k) record lists Pride Health Care, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STAIR VEYOR?

The FDA product code for STAIR VEYOR is ILK.

Related Clinical Trials

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Other records listing Pride Health Care, 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.

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Related Devices (Code: ILK)

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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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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