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)

FA TISSUE FIXATIVE & WASH SET

K-Number: K761138 · 1978-01-06

ApplicantZeus Scientific, Inc.
Decision Date1978-01-06
Product CodeLDZ
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

FA TISSUE FIXATIVE & WASH SET is the device name listed in this FDA 510(k) record. The listed applicant is Zeus Scientific, Inc.. It received FDA 510(k) clearance on 1978-01-06 under 510(k) number K761138. The device is classified under product code LDZ. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FA TISSUE FIXATIVE & WASH SET?

FA TISSUE FIXATIVE & WASH SET is a medical device that received FDA 510(k) clearance on 1978-01-06. The listed applicant is Zeus Scientific, Inc.. The 510(k) number is K761138.

When did FA TISSUE FIXATIVE & WASH SET receive FDA 510(k) clearance?

FA TISSUE FIXATIVE & WASH SET received FDA 510(k) clearance on 1978-01-06, under 510(k) number K761138.

Who is the listed applicant for FA TISSUE FIXATIVE & WASH SET?

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

What is the FDA product code for FA TISSUE FIXATIVE & WASH SET?

The FDA product code for FA TISSUE FIXATIVE & WASH SET is LDZ.

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 Zeus Scientific, 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.

K201956Zeus IFA ANA HEp-2 Test System, Zeus dIFineK191240ZEUS ELISA Borrelia VlsE1/pepC10 IgG/IgM Test System; ZEUS ELISA Borrelia burgdorferi IgM Test SystemK190907ZEUS ELISA Borrelia VlsE1/pepC10 IgG/IgM Test System; ZEUS ELISA Borrelia burgdorferi IgG/IgM Test SystemK191398ZEUS ELISA Borrelia VlsE1/pepC10 IgG/IgM Test System; ZEUS ELISA Borrelia burgdorferi IgG Test SystemK113397ZEUS ELISA BORRELIA VLSE-1/PEPC10 IGG/IGM TEST SYSTEMK102425ZEUS ELISA CARDIOLIPIN IGG/IGM/IGA TEST SYSTEM

View all 135 devices →

Related Devices (Code: LDZ)

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.

K883048ATS PARA-SET MODIFIED PVA FIXATIVE SOLUTIONAlpha-Tec Systems, Inc.K881922CYTOJARS PREFILLED WITH CYTOLOGY PRESERVATIVESurgipath Medical Industries, Inc.K881698ATS PVA FIXATIVE SOLUTIONAlpha-Tec Systems, Inc.K862725SACCOMANNO SPECIMAN SOLUTIONMill-Rose LaboratoryK843428BIOFIXAccra Laboratories, Inc.K842913WRIGHT STAIN FIXATIVEE K Ind., 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.

↑