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FDA 510(k)

XRT 600 R/F, WRF 0600

K-Number: K992603 · 1999-10-25

ApplicantWuestec Medical, Inc.
Decision Date1999-10-25
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

XRT 600 R/F, WRF 0600 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 1999-10-25 under 510(k) number K992603. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the XRT 600 R/F, WRF 0600?

XRT 600 R/F, WRF 0600 is a medical device that received FDA 510(k) clearance on 1999-10-25. The listed applicant is Wuestec Medical, Inc.. The 510(k) number is K992603.

When did XRT 600 R/F, WRF 0600 receive FDA 510(k) clearance?

XRT 600 R/F, WRF 0600 received FDA 510(k) clearance on 1999-10-25, under 510(k) number K992603.

Who is the listed applicant for XRT 600 R/F, WRF 0600?

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 XRT 600 R/F, WRF 0600?

The FDA product code for XRT 600 R/F, WRF 0600 is JAA.

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 WWS6100K992103C-QUESTK981880DX-480, ADD ON DIGITAL IMAGERK974240LIGHTLINE-MK960083MOVABLE CANTILEVERED RADIOGRAPHIC TABLE XRT 100, 200 & 300K955414XRT 400

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Related Devices (Code: JAA)

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.

K253103Nexus DRF Digital X-ray Imaging SystemVarex Imaging CorporationK251650Insight Enhanced™ DRF (EN-1002-01)Imaging Engineering, LLCK242488Soteria E-ViewOmega Medical Imaging, LLCK242948Adora DRFi (04550010)Nrt X-Ray A/SK233380TRIDENT Mobile Fluoroscopy SystemDornier Medtech AmericaK233945ProxiDiagnost N90 / Precision CRF (706110, 706400)Philips Medical Systems Dmc GmbH

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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