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FDA 510(k)

TULIP DISPOSABLE CANNULAS

K-Number: K060089 · 2006-04-27

ApplicantCell Bio-Systems, Inc.
Decision Date2006-04-27
Product CodeQPB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TULIP DISPOSABLE CANNULAS is the device name listed in this FDA 510(k) record. The listed applicant is Cell Bio-Systems, Inc.. It received FDA 510(k) clearance on 2006-04-27 under 510(k) number K060089. The device is classified under product code QPB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TULIP DISPOSABLE CANNULAS?

TULIP DISPOSABLE CANNULAS is a medical device that received FDA 510(k) clearance on 2006-04-27. The listed applicant is Cell Bio-Systems, Inc.. The 510(k) number is K060089.

When did TULIP DISPOSABLE CANNULAS receive FDA 510(k) clearance?

TULIP DISPOSABLE CANNULAS received FDA 510(k) clearance on 2006-04-27, under 510(k) number K060089.

Who is the listed applicant for TULIP DISPOSABLE CANNULAS?

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

What is the FDA product code for TULIP DISPOSABLE CANNULAS?

The FDA product code for TULIP DISPOSABLE CANNULAS is QPB.

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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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