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FDA 510(k)

MEDTEC AUTOBLOT 2000

K-Number: K951753 · 1995-10-17

ApplicantMedtec, Inc.
Decision Date1995-10-17
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MEDTEC AUTOBLOT 2000 is the device name listed in this FDA 510(k) record. The listed applicant is Medtec, Inc.. It received FDA 510(k) clearance on 1995-10-17 under 510(k) number K951753. 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 MEDTEC AUTOBLOT 2000?

MEDTEC AUTOBLOT 2000 is a medical device that received FDA 510(k) clearance on 1995-10-17. The listed applicant is Medtec, Inc.. The 510(k) number is K951753.

When did MEDTEC AUTOBLOT 2000 receive FDA 510(k) clearance?

MEDTEC AUTOBLOT 2000 received FDA 510(k) clearance on 1995-10-17, under 510(k) number K951753.

Who is the listed applicant for MEDTEC AUTOBLOT 2000?

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

What is the FDA product code for MEDTEC AUTOBLOT 2000?

The FDA product code for MEDTEC AUTOBLOT 2000 is JQW.

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Other records listing Medtec, Inc. 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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