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FDA 510(k)

MODEL ALPHA TS-2

K-Number: K935004 · 1993-12-13

ApplicantDpa Consulting, Inc.
Decision Date1993-12-13
Product CodeIYB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODEL ALPHA TS-2 is the device name listed in this FDA 510(k) record. The listed applicant is Dpa Consulting, Inc.. It received FDA 510(k) clearance on 1993-12-13 under 510(k) number K935004. The device is classified under product code IYB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL ALPHA TS-2?

MODEL ALPHA TS-2 is a medical device that received FDA 510(k) clearance on 1993-12-13. The listed applicant is Dpa Consulting, Inc.. The 510(k) number is K935004.

When did MODEL ALPHA TS-2 receive FDA 510(k) clearance?

MODEL ALPHA TS-2 received FDA 510(k) clearance on 1993-12-13, under 510(k) number K935004.

Who is the listed applicant for MODEL ALPHA TS-2?

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

What is the FDA product code for MODEL ALPHA TS-2?

The FDA product code for MODEL ALPHA TS-2 is IYB.

Related Clinical Trials

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Related Devices (Code: IYB)

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.

K935123SUPERSTAND 300Wuestec Medical, Inc.K946261MTS-007, STS-008, SSMTS-010, EURO-40, 72, SUPER EURO 4072, 5000Scott Imaging Intl., Inc.K941017F/C/W TUBESTANDAcoma Medical Imaging, Inc.K941004CTS SYSTEMAcoma Medical Imaging, Inc.K940442MPR-814Xri, Inc.K933253SUPERSTAND 3000Wuestec Medical, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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