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FDA 510(k)

SIDEKICK II

K-Number: K931231 · 1994-05-05

ApplicantPride Health Care, Inc.
Decision Date1994-05-05
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent for Some Indications

Device Summary

SIDEKICK II 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 1994-05-05 under 510(k) number K931231. The device is classified under product code INI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the SIDEKICK II?

SIDEKICK II is a medical device that received FDA 510(k) clearance on 1994-05-05. The listed applicant is Pride Health Care, Inc.. The 510(k) number is K931231.

When did SIDEKICK II receive FDA 510(k) clearance?

SIDEKICK II received FDA 510(k) clearance on 1994-05-05, under 510(k) number K931231.

Who is the listed applicant for SIDEKICK II?

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 SIDEKICK II?

The FDA product code for SIDEKICK II 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 SC445K926499SHUTTLE SC-140

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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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