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FDA 510(k)

PULL TAB SQUEEZE FLUSH

K-Number: K070979 · 2007-09-19

ApplicantIcu Medical, Inc.
Decision Date2007-09-19
Product CodeKRA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PULL TAB SQUEEZE FLUSH is the device name listed in this FDA 510(k) record. The listed applicant is Icu Medical, Inc.. It received FDA 510(k) clearance on 2007-09-19 under 510(k) number K070979. The device is classified under product code KRA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PULL TAB SQUEEZE FLUSH?

PULL TAB SQUEEZE FLUSH is a medical device that received FDA 510(k) clearance on 2007-09-19. The listed applicant is Icu Medical, Inc.. The 510(k) number is K070979.

When did PULL TAB SQUEEZE FLUSH receive FDA 510(k) clearance?

PULL TAB SQUEEZE FLUSH received FDA 510(k) clearance on 2007-09-19, under 510(k) number K070979.

Who is the listed applicant for PULL TAB SQUEEZE FLUSH?

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

What is the FDA product code for PULL TAB SQUEEZE FLUSH?

The FDA product code for PULL TAB SQUEEZE FLUSH is KRA.

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Related Devices (Code: KRA)

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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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