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FDA 510(k)

CELEBRITY XL SC445

K-Number: K944939 · 1994-11-07

Decision Date1994-11-07
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CELEBRITY XL SC445 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 1994-11-07 under 510(k) number K944939. 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 CELEBRITY XL SC445?

CELEBRITY XL SC445 is a medical device that received FDA 510(k) clearance on 1994-11-07. The listed applicant is Pride Health Care, Inc.. The 510(k) number is K944939.

When did CELEBRITY XL SC445 receive FDA 510(k) clearance?

CELEBRITY XL SC445 received FDA 510(k) clearance on 1994-11-07, under 510(k) number K944939.

Who is the listed applicant for CELEBRITY XL SC445?

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 CELEBRITY XL SC445?

The FDA product code for CELEBRITY XL SC445 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.

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