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FDA 510(k)

CELSITE/ CELSITE CONCEPT, ACCESS PORTS

K-Number: K061424 · 2006-07-31

ApplicantAesculap, Inc.
Decision Date2006-07-31
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CELSITE/ CELSITE CONCEPT, ACCESS PORTS is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 2006-07-31 under 510(k) number K061424. The device is classified under product code LJT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CELSITE/ CELSITE CONCEPT, ACCESS PORTS?

CELSITE/ CELSITE CONCEPT, ACCESS PORTS is a medical device that received FDA 510(k) clearance on 2006-07-31. The listed applicant is Aesculap, Inc.. The 510(k) number is K061424.

When did CELSITE/ CELSITE CONCEPT, ACCESS PORTS receive FDA 510(k) clearance?

CELSITE/ CELSITE CONCEPT, ACCESS PORTS received FDA 510(k) clearance on 2006-07-31, under 510(k) number K061424.

Who is the listed applicant for CELSITE/ CELSITE CONCEPT, ACCESS PORTS?

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

What is the FDA product code for CELSITE/ CELSITE CONCEPT, ACCESS PORTS?

The FDA product code for CELSITE/ CELSITE CONCEPT, ACCESS PORTS is LJT.

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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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