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FDA 510(k)

PROBE(TM) MODELS 700 AND 1000

K-Number: K883749 · 1988-11-10

ApplicantPackard Instrument Co., Inc.
Decision Date1988-11-10
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PROBE(TM) MODELS 700 AND 1000 is the device name listed in this FDA 510(k) record. The listed applicant is Packard Instrument Co., Inc.. It received FDA 510(k) clearance on 1988-11-10 under 510(k) number K883749. 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 PROBE(TM) MODELS 700 AND 1000?

PROBE(TM) MODELS 700 AND 1000 is a medical device that received FDA 510(k) clearance on 1988-11-10. The listed applicant is Packard Instrument Co., Inc.. The 510(k) number is K883749.

When did PROBE(TM) MODELS 700 AND 1000 receive FDA 510(k) clearance?

PROBE(TM) MODELS 700 AND 1000 received FDA 510(k) clearance on 1988-11-10, under 510(k) number K883749.

Who is the listed applicant for PROBE(TM) MODELS 700 AND 1000?

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

What is the FDA product code for PROBE(TM) MODELS 700 AND 1000?

The FDA product code for PROBE(TM) MODELS 700 AND 1000 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 Packard Instrument Co., 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.

K924907FILTERMATE UNIVERSAL HARVESTERK913664ROSYS MODELS 100 AND 200K901808MICROMATE 196 MODEL A961960

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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