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FDA 510(k)

QL LOCKING SYRINGE

K-Number: K060643 · 2006-07-12

ApplicantAtrion Medical Products, Inc.
Decision Date2006-07-12
Product CodeMAV
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

QL LOCKING SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Atrion Medical Products, Inc.. It received FDA 510(k) clearance on 2006-07-12 under 510(k) number K060643. The device is classified under product code MAV. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QL LOCKING SYRINGE?

QL LOCKING SYRINGE is a medical device that received FDA 510(k) clearance on 2006-07-12. The listed applicant is Atrion Medical Products, Inc.. The 510(k) number is K060643.

When did QL LOCKING SYRINGE receive FDA 510(k) clearance?

QL LOCKING SYRINGE received FDA 510(k) clearance on 2006-07-12, under 510(k) number K060643.

Who is the listed applicant for QL LOCKING SYRINGE?

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

What is the FDA product code for QL LOCKING SYRINGE?

The FDA product code for QL LOCKING SYRINGE is MAV.

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Related Devices (Code: MAV)

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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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