FDA 510(k)

37% FORMALDEHYDE

K-Number: K811794 · 1981-07-28

ApplicantRichard-Allan Medical Ind., Inc.

Decision Date1981-07-28

Product CodeIGG

Advisory CommitteePA

DecisionSubstantially Equivalent

Device Summary

37% FORMALDEHYDE is the device name listed in this FDA 510(k) record. The listed applicant is Richard-Allan Medical Ind., Inc.. It received FDA 510(k) clearance on 1981-07-28 under 510(k) number K811794. The device is classified under product code IGG. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 37% FORMALDEHYDE?

37% FORMALDEHYDE is a medical device that received FDA 510(k) clearance on 1981-07-28. The listed applicant is Richard-Allan Medical Ind., Inc.. The 510(k) number is K811794.

When did 37% FORMALDEHYDE receive FDA 510(k) clearance?

37% FORMALDEHYDE received FDA 510(k) clearance on 1981-07-28, under 510(k) number K811794.

Who is the listed applicant for 37% FORMALDEHYDE?

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

What is the FDA product code for 37% FORMALDEHYDE?

The FDA product code for 37% FORMALDEHYDE is IGG.

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Other records listing Richard-Allan Medical Ind., Inc. as applicant

K931879REFLEX HTR K924200REFLEX(R) ESC K926297REFLEX ESI K924761STERILE ENDOSCOPIC DISPOS TROCARS W/SAFE SHIELD K900566RICHARD-ALLAN VESSEL LOOPS K896262TITANIUM LIGATING CLIPS

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Related Devices (Code: IGG)

K882268ZINC FORMALIN CONCENTRATEAnatech, Ltd.K861201FORMALDEHYDE SOLUTION, 37%Surgipath Medical Industries, Inc.K802506PLEASCENT OR FORMA-SCENTMeridian Diagnostics, Inc.K792707PARA-PAK SAFMeridian Diagnostics, Inc.K792705PARA-PAK FORMALINMeridian Diagnostics, Inc.K771201FORMALIN BUFFER CONCENTRATECentral Labs. Assoc. MD Pathologists

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.