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FDA 510(k)

FORMALIN BUFFER CONCENTRATE

K-Number: K771201 · 1977-08-22

ApplicantCentral Labs. Assoc. MD Pathologists
Decision Date1977-08-22
Product CodeIGG
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

FORMALIN BUFFER CONCENTRATE is the device name listed in this FDA 510(k) record. The listed applicant is Central Labs. Assoc. MD Pathologists. It received FDA 510(k) clearance on 1977-08-22 under 510(k) number K771201. 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 FORMALIN BUFFER CONCENTRATE?

FORMALIN BUFFER CONCENTRATE is a medical device that received FDA 510(k) clearance on 1977-08-22. The listed applicant is Central Labs. Assoc. MD Pathologists. The 510(k) number is K771201.

When did FORMALIN BUFFER CONCENTRATE receive FDA 510(k) clearance?

FORMALIN BUFFER CONCENTRATE received FDA 510(k) clearance on 1977-08-22, under 510(k) number K771201.

Who is the listed applicant for FORMALIN BUFFER CONCENTRATE?

The FDA 510(k) record lists Central Labs. Assoc. MD Pathologists as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FORMALIN BUFFER CONCENTRATE?

The FDA product code for FORMALIN BUFFER CONCENTRATE is IGG.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Central Labs. Assoc. MD Pathologists 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.

K761183LYSING AGENT AFK761182ISOTONIC DILUENT AF

Related Devices (Code: IGG)

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.

K882268ZINC FORMALIN CONCENTRATEAnatech, Ltd.K861201FORMALDEHYDE SOLUTION, 37%Surgipath Medical Industries, Inc.K81179437% FORMALDEHYDERichard-Allan Medical Ind., Inc.K802506PLEASCENT OR FORMA-SCENTMeridian Diagnostics, Inc.K792707PARA-PAK SAFMeridian Diagnostics, Inc.K792705PARA-PAK FORMALINMeridian Diagnostics, Inc.

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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