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FDA 510(k)

CAROLINA X-RAY CO. SIMPLAFLOAT TABLE

K-Number: K842614 · 1984-08-08

ApplicantCarolina X-Ray Co., Inc.
Decision Date1984-08-08
Product CodeIXQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CAROLINA X-RAY CO. SIMPLAFLOAT TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Carolina X-Ray Co., Inc.. It received FDA 510(k) clearance on 1984-08-08 under 510(k) number K842614. The device is classified under product code IXQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAROLINA X-RAY CO. SIMPLAFLOAT TABLE?

CAROLINA X-RAY CO. SIMPLAFLOAT TABLE is a medical device that received FDA 510(k) clearance on 1984-08-08. The listed applicant is Carolina X-Ray Co., Inc.. The 510(k) number is K842614.

When did CAROLINA X-RAY CO. SIMPLAFLOAT TABLE receive FDA 510(k) clearance?

CAROLINA X-RAY CO. SIMPLAFLOAT TABLE received FDA 510(k) clearance on 1984-08-08, under 510(k) number K842614.

Who is the listed applicant for CAROLINA X-RAY CO. SIMPLAFLOAT TABLE?

The FDA 510(k) record lists Carolina X-Ray Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CAROLINA X-RAY CO. SIMPLAFLOAT TABLE?

The FDA product code for CAROLINA X-RAY CO. SIMPLAFLOAT TABLE is IXQ.

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Related Devices (Code: IXQ)

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.

K973842CARBON FIBER CONFORMAL COUCH TOPMedtec, Inc.K960083MOVABLE CANTILEVERED RADIOGRAPHIC TABLE XRT 100, 200 & 300Wuestec Medical, Inc.K954225MED-TEC HAND GRIPMedtec, Inc.K946262EURO, SCST, SCCFT ATLAS RADIOLOGIC TABLESScott Imaging Intl., Inc.K942916OCTOPAQUE UNIVERSALOctostop, Inc.K942190ID100 MOBILE FLUOROSCOPIC EXAMINING TABLEImage Diagnostics, 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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