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FDA 510(k)

IMMUNO-WASH AUTOMATED TUBE WASHER

K-Number: K893810 · 1989-08-03

ApplicantOcean Scientific, Inc.
Decision Date1989-08-03
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

IMMUNO-WASH AUTOMATED TUBE WASHER is the device name listed in this FDA 510(k) record. The listed applicant is Ocean Scientific, Inc.. It received FDA 510(k) clearance on 1989-08-03 under 510(k) number K893810. The device is classified under product code JQW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMMUNO-WASH AUTOMATED TUBE WASHER?

IMMUNO-WASH AUTOMATED TUBE WASHER is a medical device that received FDA 510(k) clearance on 1989-08-03. The listed applicant is Ocean Scientific, Inc.. The 510(k) number is K893810.

When did IMMUNO-WASH AUTOMATED TUBE WASHER receive FDA 510(k) clearance?

IMMUNO-WASH AUTOMATED TUBE WASHER received FDA 510(k) clearance on 1989-08-03, under 510(k) number K893810.

Who is the listed applicant for IMMUNO-WASH AUTOMATED TUBE WASHER?

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

What is the FDA product code for IMMUNO-WASH AUTOMATED TUBE WASHER?

The FDA product code for IMMUNO-WASH AUTOMATED TUBE WASHER is JQW.

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 Ocean 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.

K873638MICRO-CHEM ANALYZERK864731OCEAN SCIENTIFIC VDRL TESTK863976OCEAN SCIENTIFIC VACUTESTK860987MINI-CHEM ANALYZERK840340CHEM-STAT ANALYZER

Related Devices (Code: JQW)

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.

K023955BD VIPER INSTRUMENTBecton, Dickinson & COK973335QUATRO SP SAMPLE PROCESSING SYSTEMS (200-499, INCLUSIVE)Zenyx Scientific , Ltd.K9801802700 SAMPLE MANAGERWaters CorporationK970420MASTERCAP AM 5.0/MASTERCAP RM 5.0Pharmacia, Inc.K970616MINI SAMPLER PROCESSORCavro Scientific Instruments, Inc.K962687GIO. DE VITA E C. S.R.L.(GDV) AUTOMATIC WASHING SYSTEMNichols Institute Diagnostics

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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