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FDA 510(k)

HYDROL

K-Number: K760660 · 1976-09-27

ApplicantSeptodont, Inc.
Decision Date1976-09-27
Product CodeLBH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

HYDROL is the device name listed in this FDA 510(k) record. The listed applicant is Septodont, Inc.. It received FDA 510(k) clearance on 1976-09-27 under 510(k) number K760660. The device is classified under product code LBH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYDROL?

HYDROL is a medical device that received FDA 510(k) clearance on 1976-09-27. The listed applicant is Septodont, Inc.. The 510(k) number is K760660.

When did HYDROL receive FDA 510(k) clearance?

HYDROL received FDA 510(k) clearance on 1976-09-27, under 510(k) number K760660.

Who is the listed applicant for HYDROL?

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

What is the FDA product code for HYDROL?

The FDA product code for HYDROL is LBH.

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Related PubMed Literature

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PMID: 33050694Unravelling the Immunotoxicity of Polycaprolactone Nanoparticles-Effects of Polymer Molecular Weight, Hydrolysis, and Blends.Chemical research in toxicology ()

Other records listing Septodont, 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.

K780003ENDOSOLV EK771114NEUTROCIMK761354CIMPAT (PINK AND WHITE)K761355SELFASTK760798FLUOCAL GEL MINTK760799FLUOCAL GEL ORANGE

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Related Devices (Code: LBH)

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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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