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FDA 510(k)

BLACKSTONE ASCENT POCT SYSTEM HOOKS (SYSTEM MODIFICATION)

K-Number: K033980 · 2004-03-03

Decision Date2004-03-03
Product CodeKWP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BLACKSTONE ASCENT POCT SYSTEM HOOKS (SYSTEM MODIFICATION) is the device name listed in this FDA 510(k) record. The listed applicant is Blackstone Medical, Inc.. It received FDA 510(k) clearance on 2004-03-03 under 510(k) number K033980. The device is classified under product code KWP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLACKSTONE ASCENT POCT SYSTEM HOOKS (SYSTEM MODIFICATION)?

BLACKSTONE ASCENT POCT SYSTEM HOOKS (SYSTEM MODIFICATION) is a medical device that received FDA 510(k) clearance on 2004-03-03. The listed applicant is Blackstone Medical, Inc.. The 510(k) number is K033980.

When did BLACKSTONE ASCENT POCT SYSTEM HOOKS (SYSTEM MODIFICATION) receive FDA 510(k) clearance?

BLACKSTONE ASCENT POCT SYSTEM HOOKS (SYSTEM MODIFICATION) received FDA 510(k) clearance on 2004-03-03, under 510(k) number K033980.

Who is the listed applicant for BLACKSTONE ASCENT POCT SYSTEM HOOKS (SYSTEM MODIFICATION)?

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

What is the FDA product code for BLACKSTONE ASCENT POCT SYSTEM HOOKS (SYSTEM MODIFICATION)?

The FDA product code for BLACKSTONE ASCENT POCT SYSTEM HOOKS (SYSTEM MODIFICATION) is KWP.

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 Blackstone Medical, 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 45 devices →

Related Devices (Code: KWP)

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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