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FDA 510(k)

PRO QUANTUM

K-Number: K831249 · 1983-07-28

ApplicantAbbott Laboratories
Decision Date1983-07-28
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PRO QUANTUM is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1983-07-28 under 510(k) number K831249. 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 PRO QUANTUM?

PRO QUANTUM is a medical device that received FDA 510(k) clearance on 1983-07-28. The listed applicant is Abbott Laboratories. The 510(k) number is K831249.

When did PRO QUANTUM receive FDA 510(k) clearance?

PRO QUANTUM received FDA 510(k) clearance on 1983-07-28, under 510(k) number K831249.

Who is the listed applicant for PRO QUANTUM?

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

What is the FDA product code for PRO QUANTUM?

The FDA product code for PRO QUANTUM is JQW.

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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.

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Other records listing Abbott Laboratories as applicant

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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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