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FDA 510(k)

AVOCET SYSTEM LIQUID CONTROL LEVEL 1 AND LEVEL 2

K-Number: K980982 · 1998-04-16

ApplicantAvocet Medical, Inc.
Decision Date1998-04-16
Product CodeGGN
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

AVOCET SYSTEM LIQUID CONTROL LEVEL 1 AND LEVEL 2 is the device name listed in this FDA 510(k) record. The listed applicant is Avocet Medical, Inc.. It received FDA 510(k) clearance on 1998-04-16 under 510(k) number K980982. The device is classified under product code GGN. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AVOCET SYSTEM LIQUID CONTROL LEVEL 1 AND LEVEL 2?

AVOCET SYSTEM LIQUID CONTROL LEVEL 1 AND LEVEL 2 is a medical device that received FDA 510(k) clearance on 1998-04-16. The listed applicant is Avocet Medical, Inc.. The 510(k) number is K980982.

When did AVOCET SYSTEM LIQUID CONTROL LEVEL 1 AND LEVEL 2 receive FDA 510(k) clearance?

AVOCET SYSTEM LIQUID CONTROL LEVEL 1 AND LEVEL 2 received FDA 510(k) clearance on 1998-04-16, under 510(k) number K980982.

Who is the listed applicant for AVOCET SYSTEM LIQUID CONTROL LEVEL 1 AND LEVEL 2?

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

What is the FDA product code for AVOCET SYSTEM LIQUID CONTROL LEVEL 1 AND LEVEL 2?

The FDA product code for AVOCET SYSTEM LIQUID CONTROL LEVEL 1 AND LEVEL 2 is GGN.

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Other records listing Avocet Medical, 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.

K994006AVOCET ACUSURE (FOR PATIENT SELF-TESTING) AND AVOCET ACUSURE PRO (FOR PROFESSIONAL USE)K991286AVOCET ACUSURE SYSTEMK980839AVOCET PT

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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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