Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

PRIDE LEGEND SC-340

K-Number: K930952 · 1994-03-28

Decision Date1994-03-28
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent for Some Indications

Device Summary

PRIDE LEGEND SC-340 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 1994-03-28 under 510(k) number K930952. 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 PRIDE LEGEND SC-340?

PRIDE LEGEND SC-340 is a medical device that received FDA 510(k) clearance on 1994-03-28. The listed applicant is Pride Health Care, Inc.. The 510(k) number is K930952.

When did PRIDE LEGEND SC-340 receive FDA 510(k) clearance?

PRIDE LEGEND SC-340 received FDA 510(k) clearance on 1994-03-28, under 510(k) number K930952.

Who is the listed applicant for PRIDE LEGEND SC-340?

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 LEGEND SC-340?

The FDA product code for PRIDE LEGEND SC-340 is INI.

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.

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.

View all 19 devices →

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.

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.

↑