Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

LIQUA-SONIC GEL

K-Number: K841871 · 1985-03-14

Decision Date1985-03-14
Product CodeGYB
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

LIQUA-SONIC GEL is the device name listed in this FDA 510(k) record. The listed applicant is Chester Labs, Inc.. It received FDA 510(k) clearance on 1985-03-14 under 510(k) number K841871. The device is classified under product code GYB. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 11 devices →

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.

↑