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FDA 510(k)

AFFIRM PROCESSOR

K-Number: K923268 · 1992-07-30

ApplicantMicroprobe Corp.
Decision Date1992-07-30
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

AFFIRM PROCESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Microprobe Corp.. It received FDA 510(k) clearance on 1992-07-30 under 510(k) number K923268. 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 AFFIRM PROCESSOR?

AFFIRM PROCESSOR is a medical device that received FDA 510(k) clearance on 1992-07-30. The listed applicant is Microprobe Corp.. The 510(k) number is K923268.

When did AFFIRM PROCESSOR receive FDA 510(k) clearance?

AFFIRM PROCESSOR received FDA 510(k) clearance on 1992-07-30, under 510(k) number K923268.

Who is the listed applicant for AFFIRM PROCESSOR?

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

What is the FDA product code for AFFIRM PROCESSOR?

The FDA product code for AFFIRM PROCESSOR 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 Microprobe Corp. 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.

K931151AFFIRM(TM) VPIII MICROBIAL IDENT TEST FOR CANDIDAK931374AFFIRM VPIII MICROBIAL IDENTIFICATION TESTK922457AFFIRM VP MICROBIAL ID TEST FOR TRICHOMONAS VAGINAK923133AFFIRM/VP IDENT.TEST G.VAGINALIS & T.VAGINALISK920536AFFIRM VP SAMPLE COLLECTION SET

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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