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FDA 510(k)

STARS2000 POWER CANNULA

K-Number: K012236 · 2001-11-19

ApplicantKmi Kolster Methods, Inc.
Decision Date2001-11-19
Product CodeQPB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STARS2000 POWER CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Kmi Kolster Methods, Inc.. It received FDA 510(k) clearance on 2001-11-19 under 510(k) number K012236. 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 STARS2000 POWER CANNULA?

STARS2000 POWER CANNULA is a medical device that received FDA 510(k) clearance on 2001-11-19. The listed applicant is Kmi Kolster Methods, Inc.. The 510(k) number is K012236.

When did STARS2000 POWER CANNULA receive FDA 510(k) clearance?

STARS2000 POWER CANNULA received FDA 510(k) clearance on 2001-11-19, under 510(k) number K012236.

Who is the listed applicant for STARS2000 POWER CANNULA?

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

What is the FDA product code for STARS2000 POWER CANNULA?

The FDA product code for STARS2000 POWER CANNULA is QPB.

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Other records listing Kmi Kolster Methods, 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.

K060414KOLSTER METHODS, INC., FEATHERLIFT SILHOUETTE SUTUREK043591FEATHERLIFT EXTENDED APTOS THREADK010702XUB EXTERNAL ULTRASOUNDK002859SSW-STERILE SOLUTION WARMERK991203IRRIGATION OR INFUSION PUMP K PUMP

Related Devices (Code: QPB)

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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