LIQUA-SONIC GEL
K-Number: K841871 · 1985-03-14
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Device Summary
Frequently Asked Questions
What is the LIQUA-SONIC GEL?
LIQUA-SONIC GEL is a medical device that received FDA 510(k) clearance on 1985-03-14. The listed applicant is Chester Labs, Inc.. The 510(k) number is K841871.
When did LIQUA-SONIC GEL receive FDA 510(k) clearance?
LIQUA-SONIC GEL received FDA 510(k) clearance on 1985-03-14, under 510(k) number K841871.
Who is the listed applicant for LIQUA-SONIC GEL?
The FDA 510(k) record lists Chester Labs, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIQUA-SONIC GEL?
The FDA product code for LIQUA-SONIC GEL is GYB.
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 Chester Labs, 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: GYB)
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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