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FDA 510(k)

PRIDE SPIRIT

K-Number: K905271 · 1990-12-31

ApplicantPride Health Care, Inc.
Decision Date1990-12-31
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PRIDE SPIRIT 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 1990-12-31 under 510(k) number K905271. The device is classified under product code INI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRIDE SPIRIT?

PRIDE SPIRIT is a medical device that received FDA 510(k) clearance on 1990-12-31. The listed applicant is Pride Health Care, Inc.. The 510(k) number is K905271.

When did PRIDE SPIRIT receive FDA 510(k) clearance?

PRIDE SPIRIT received FDA 510(k) clearance on 1990-12-31, under 510(k) number K905271.

Who is the listed applicant for PRIDE SPIRIT?

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 PRIDE SPIRIT?

The FDA product code for PRIDE SPIRIT is INI.

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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.

K945936JAZZYK944940EURO SC500K953342TMR48K944277DYNAMOK944939CELEBRITY XL SC445K931231SIDEKICK II

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Related Devices (Code: INI)

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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