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FDA 510(k)

SUPER SPEED POTTER-BUCKY (ESO5-110 & 220)

K-Number: K893690 · 1989-07-20

ApplicantHofmann X-Ray of America, Inc.
Decision Date1989-07-20
Product CodeIXQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SUPER SPEED POTTER-BUCKY (ESO5-110 & 220) is the device name listed in this FDA 510(k) record. The listed applicant is Hofmann X-Ray of America, Inc.. It received FDA 510(k) clearance on 1989-07-20 under 510(k) number K893690. 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 SUPER SPEED POTTER-BUCKY (ESO5-110 & 220)?

SUPER SPEED POTTER-BUCKY (ESO5-110 & 220) is a medical device that received FDA 510(k) clearance on 1989-07-20. The listed applicant is Hofmann X-Ray of America, Inc.. The 510(k) number is K893690.

When did SUPER SPEED POTTER-BUCKY (ESO5-110 & 220) receive FDA 510(k) clearance?

SUPER SPEED POTTER-BUCKY (ESO5-110 & 220) received FDA 510(k) clearance on 1989-07-20, under 510(k) number K893690.

Who is the listed applicant for SUPER SPEED POTTER-BUCKY (ESO5-110 & 220)?

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

What is the FDA product code for SUPER SPEED POTTER-BUCKY (ESO5-110 & 220)?

The FDA product code for SUPER SPEED POTTER-BUCKY (ESO5-110 & 220) is IXQ.

Related Clinical Trials

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Other records listing Hofmann X-Ray of America, 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.

K851011HOFMANN G-S60 SINGLE PHASE X-RAY GENERATOR

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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