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FDA 510(k)

CARBON MEDICAL TECHNOLOGIES ENDOSCOPIC INJECTION NEEDLE

K-Number: K042615 · 2004-11-05

Decision Date2004-11-05
Product CodeFBK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CARBON MEDICAL TECHNOLOGIES ENDOSCOPIC INJECTION NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Carbon Medical Technologies, Inc.. It received FDA 510(k) clearance on 2004-11-05 under 510(k) number K042615. The device is classified under product code FBK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARBON MEDICAL TECHNOLOGIES ENDOSCOPIC INJECTION NEEDLE?

CARBON MEDICAL TECHNOLOGIES ENDOSCOPIC INJECTION NEEDLE is a medical device that received FDA 510(k) clearance on 2004-11-05. The listed applicant is Carbon Medical Technologies, Inc.. The 510(k) number is K042615.

When did CARBON MEDICAL TECHNOLOGIES ENDOSCOPIC INJECTION NEEDLE receive FDA 510(k) clearance?

CARBON MEDICAL TECHNOLOGIES ENDOSCOPIC INJECTION NEEDLE received FDA 510(k) clearance on 2004-11-05, under 510(k) number K042615.

Who is the listed applicant for CARBON MEDICAL TECHNOLOGIES ENDOSCOPIC INJECTION NEEDLE?

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

What is the FDA product code for CARBON MEDICAL TECHNOLOGIES ENDOSCOPIC INJECTION NEEDLE?

The FDA product code for CARBON MEDICAL TECHNOLOGIES ENDOSCOPIC INJECTION NEEDLE is FBK.

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 Carbon Medical Technologies, 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 15 devices →

Related Devices (Code: FBK)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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