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FDA 510(k)

STAT FAX 2600

K-Number: K941394 · 1994-06-03

ApplicantAwareness Technology, Inc.
Decision Date1994-06-03
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

STAT FAX 2600 is the device name listed in this FDA 510(k) record. The listed applicant is Awareness Technology, Inc.. It received FDA 510(k) clearance on 1994-06-03 under 510(k) number K941394. 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 STAT FAX 2600?

STAT FAX 2600 is a medical device that received FDA 510(k) clearance on 1994-06-03. The listed applicant is Awareness Technology, Inc.. The 510(k) number is K941394.

When did STAT FAX 2600 receive FDA 510(k) clearance?

STAT FAX 2600 received FDA 510(k) clearance on 1994-06-03, under 510(k) number K941394.

Who is the listed applicant for STAT FAX 2600?

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

What is the FDA product code for STAT FAX 2600?

The FDA product code for STAT FAX 2600 is JQW.

Other records listing Awareness Technology, 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.

K171476SelectaLyte Electrolyte Analyzer (Na+, K+, Cl-)K013420CHEMWELL, ALSO KNOWN AS PROJECT 2900K010877CHEMWELL, MODEL 2900K974762STAT TRACKSK943729DYE CHECK STRIPS 545-630K923598REDI-CHECK PHOTMETER Q.A.

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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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