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FDA 510(k)

POS T-7000

K-Number: K981805 · 1998-08-07

ApplicantPos Technologies, Inc.
Decision Date1998-08-07
Product CodeHCS
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

POS T-7000 is the device name listed in this FDA 510(k) record. The listed applicant is Pos Technologies, Inc.. It received FDA 510(k) clearance on 1998-08-07 under 510(k) number K981805. The device is classified under product code HCS. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POS T-7000?

POS T-7000 is a medical device that received FDA 510(k) clearance on 1998-08-07. The listed applicant is Pos Technologies, Inc.. The 510(k) number is K981805.

When did POS T-7000 receive FDA 510(k) clearance?

POS T-7000 received FDA 510(k) clearance on 1998-08-07, under 510(k) number K981805.

Who is the listed applicant for POS T-7000?

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

What is the FDA product code for POS T-7000?

The FDA product code for POS T-7000 is HCS.

Related Devices (Code: HCS)

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.

K974208TYTRON C-3000Titronics Research & Development Co.K950986NEUROREADERArtronicsK894772THERMALGRAPHIC ANALYSERMedtech InstrumentsK840487T-METERK.J. ElectronicsK831995TRENDO-SCOPEGabriel Ent.K822795GABRIEL DIGITRENDGabriel Ent.

Official Source

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