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FDA 510(k)

SUPERSTAND 300

K-Number: K935123 · 1996-03-27

ApplicantWuestec Medical, Inc.
Decision Date1996-03-27
Product CodeIYB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SUPERSTAND 300 is the device name listed in this FDA 510(k) record. The listed applicant is Wuestec Medical, Inc.. It received FDA 510(k) clearance on 1996-03-27 under 510(k) number K935123. 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 SUPERSTAND 300?

SUPERSTAND 300 is a medical device that received FDA 510(k) clearance on 1996-03-27. The listed applicant is Wuestec Medical, Inc.. The 510(k) number is K935123.

When did SUPERSTAND 300 receive FDA 510(k) clearance?

SUPERSTAND 300 received FDA 510(k) clearance on 1996-03-27, under 510(k) number K935123.

Who is the listed applicant for SUPERSTAND 300?

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

What is the FDA product code for SUPERSTAND 300?

The FDA product code for SUPERSTAND 300 is IYB.

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Other records listing Wuestec Medical, 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.

K993962PENSIL TRAUMA, MODEL WWS6100K992603XRT 600 R/F, WRF 0600K992103C-QUESTK981880DX-480, ADD ON DIGITAL IMAGERK974240LIGHTLINE-MK955414XRT 400

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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.

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.K935004MODEL ALPHA TS-2Dpa Consulting, Inc.K933253SUPERSTAND 3000Wuestec Medical, Inc.

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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