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FDA 510(k)

CEILING MOUNTED RADIOGRAPHIC SYSTEM TRAUMEX

K-Number: K880530 · 1988-03-03

ApplicantFischer Imaging Corp.
Decision Date1988-03-03
Product CodeIYB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CEILING MOUNTED RADIOGRAPHIC SYSTEM TRAUMEX is the device name listed in this FDA 510(k) record. The listed applicant is Fischer Imaging Corp.. It received FDA 510(k) clearance on 1988-03-03 under 510(k) number K880530. 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 CEILING MOUNTED RADIOGRAPHIC SYSTEM TRAUMEX?

CEILING MOUNTED RADIOGRAPHIC SYSTEM TRAUMEX is a medical device that received FDA 510(k) clearance on 1988-03-03. The listed applicant is Fischer Imaging Corp.. The 510(k) number is K880530.

When did CEILING MOUNTED RADIOGRAPHIC SYSTEM TRAUMEX receive FDA 510(k) clearance?

CEILING MOUNTED RADIOGRAPHIC SYSTEM TRAUMEX received FDA 510(k) clearance on 1988-03-03, under 510(k) number K880530.

Who is the listed applicant for CEILING MOUNTED RADIOGRAPHIC SYSTEM TRAUMEX?

The FDA 510(k) record lists Fischer Imaging Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CEILING MOUNTED RADIOGRAPHIC SYSTEM TRAUMEX?

The FDA product code for CEILING MOUNTED RADIOGRAPHIC SYSTEM TRAUMEX is IYB.

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Other records listing Fischer Imaging Corp. 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.

K042095MAMMOTESTK021113MAMMOPATHK981414LC POSITIONERK973400MAMMOTEST ADAPTER DRIVERK964806MD-1835K961207EP-X BIPLANE

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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.K941004CTS SYSTEMAcoma Medical Imaging, Inc.K941017F/C/W TUBESTANDAcoma Medical Imaging, Inc.K940442MPR-814Xri, Inc.K935004MODEL ALPHA TS-2Dpa Consulting, 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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