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FDA 510(k)

REPROCESSED ENDOSCOPIC TROCARS AND CANNULAS

K-Number: K063788 · 2007-10-15

ApplicantAscent Healthcare Solutions
Decision Date2007-10-15
Product CodeNLM
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

REPROCESSED ENDOSCOPIC TROCARS AND CANNULAS is the device name listed in this FDA 510(k) record. The listed applicant is Ascent Healthcare Solutions. It received FDA 510(k) clearance on 2007-10-15 under 510(k) number K063788. The device is classified under product code NLM. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPROCESSED ENDOSCOPIC TROCARS AND CANNULAS?

REPROCESSED ENDOSCOPIC TROCARS AND CANNULAS is a medical device that received FDA 510(k) clearance on 2007-10-15. The listed applicant is Ascent Healthcare Solutions. The 510(k) number is K063788.

When did REPROCESSED ENDOSCOPIC TROCARS AND CANNULAS receive FDA 510(k) clearance?

REPROCESSED ENDOSCOPIC TROCARS AND CANNULAS received FDA 510(k) clearance on 2007-10-15, under 510(k) number K063788.

Who is the listed applicant for REPROCESSED ENDOSCOPIC TROCARS AND CANNULAS?

The FDA 510(k) record lists Ascent Healthcare Solutions as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REPROCESSED ENDOSCOPIC TROCARS AND CANNULAS?

The FDA product code for REPROCESSED ENDOSCOPIC TROCARS AND CANNULAS is NLM.

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Other records listing Ascent Healthcare Solutions 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.

K111600REPROCESSED HAND ACTIVATE SEALER/DIVIDERK110189REPROCESSED ELECTROSURGICAL INSTRUMENTK100909REPROCESSED COMPRESSION SLEEVESK100254REPROCESSED CS BI-DIECTIONAL DIAGNOSTIC ELECTROPHYSIOLOGY CATHETERK100537REPROCESSED ULTRASONIC CURVED SHEARS WITH TORQUE WRENCH AND GRIP ASSIST MODEL FCS9, TWBLUE, GABLUEK100080REPROCESSED TROCARS, MODEL B5LT AND CB5LT

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Related Devices (Code: NLM)

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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