CONFLUENT SURGICAL DUAL LIQUID APPLICATOR, MODEL 70-2005093
K-Number: K042588 · 2004-12-09
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Device Summary
Frequently Asked Questions
What is the CONFLUENT SURGICAL DUAL LIQUID APPLICATOR, MODEL 70-2005093?
CONFLUENT SURGICAL DUAL LIQUID APPLICATOR, MODEL 70-2005093 is a medical device that received FDA 510(k) clearance on 2004-12-09. The listed applicant is Confluent Surgical,Inc. The 510(k) number is K042588.
When did CONFLUENT SURGICAL DUAL LIQUID APPLICATOR, MODEL 70-2005093 receive FDA 510(k) clearance?
CONFLUENT SURGICAL DUAL LIQUID APPLICATOR, MODEL 70-2005093 received FDA 510(k) clearance on 2004-12-09, under 510(k) number K042588.
Who is the listed applicant for CONFLUENT SURGICAL DUAL LIQUID APPLICATOR, MODEL 70-2005093?
The FDA 510(k) record lists Confluent Surgical,Inc as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CONFLUENT SURGICAL DUAL LIQUID APPLICATOR, MODEL 70-2005093?
The FDA product code for CONFLUENT SURGICAL DUAL LIQUID APPLICATOR, MODEL 70-2005093 is FMF.
Related Clinical Trials
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.
Other records listing Confluent Surgical,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.
Related Devices (Code: FMF)
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.
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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