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FDA 510(k)

AESCULAP PRIMELINE CONTAINER LTD.

K-Number: K073168 · 2008-04-28

ApplicantAesculap, Inc.
Decision Date2008-04-28
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AESCULAP PRIMELINE CONTAINER LTD. is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 2008-04-28 under 510(k) number K073168. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AESCULAP PRIMELINE CONTAINER LTD.?

AESCULAP PRIMELINE CONTAINER LTD. is a medical device that received FDA 510(k) clearance on 2008-04-28. The listed applicant is Aesculap, Inc.. The 510(k) number is K073168.

When did AESCULAP PRIMELINE CONTAINER LTD. receive FDA 510(k) clearance?

AESCULAP PRIMELINE CONTAINER LTD. received FDA 510(k) clearance on 2008-04-28, under 510(k) number K073168.

Who is the listed applicant for AESCULAP PRIMELINE CONTAINER LTD.?

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 AESCULAP PRIMELINE CONTAINER LTD.?

The FDA product code for AESCULAP PRIMELINE CONTAINER LTD. is KCT.

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Other records listing Aesculap, Inc. as applicant

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Related Devices (Code: KCT)

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.

K253988LiteSet TraysNobel Biocare ABK261935Surgical and Prosthetic TraysDentsply Sirona, Inc.K253187SteriBest® Sterilization Tray SystemMastel SurgicalK260726Straumann® ProClean™ Cassette (041.800 ; 041.801)Institut Straumann AGK252854SteriTite Container System with MediTray ProductsCase Medical, Inc.K253791PUREVUE™ Quick Connect Cannula System Tray; PUREVUE™ Quick Connect Cannula System LidDePuy Mitek, Inc.

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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