FDA 510(k)

PATIENT INFORMATION MANAGER (PIM)

K-Number: K921986 · 1992-10-16

Decision Date1992-10-16

Product CodeIZH

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

PATIENT INFORMATION MANAGER (PIM) is the device name listed in this FDA 510(k) record. The listed applicant is Continental X-Ray Corp.. It received FDA 510(k) clearance on 1992-10-16 under 510(k) number K921986. The device is classified under product code IZH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PATIENT INFORMATION MANAGER (PIM)?

PATIENT INFORMATION MANAGER (PIM) is a medical device that received FDA 510(k) clearance on 1992-10-16. The listed applicant is Continental X-Ray Corp.. The 510(k) number is K921986.

When did PATIENT INFORMATION MANAGER (PIM) receive FDA 510(k) clearance?

PATIENT INFORMATION MANAGER (PIM) received FDA 510(k) clearance on 1992-10-16, under 510(k) number K921986.

Who is the listed applicant for PATIENT INFORMATION MANAGER (PIM)?

The FDA 510(k) record lists Continental X-Ray Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PATIENT INFORMATION MANAGER (PIM)?

The FDA product code for PATIENT INFORMATION MANAGER (PIM) is IZH.

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Other records listing Continental X-Ray Corp. as applicant

K972442CEILING MOUNTED LATERAL POSITIONER, MODEL NO. 6896.002 K962140ICT-2000, INTEGRATED C-ARM/TABLE MULTIPURPOSE RADIOGRAPHIC/FLUOROSCOPIC POSITIONING SYSTEM MODEL NO. 6896.300 K961690CARDIOARC SERIES: POSITIONER C-ARM MODELS NO. 6896.001 AND 6896.105 K954581ARC SERIES K950571LINEAR FR TOMOGRAPHIC SYSTEM: 0MT 8000, MODEL NO. 6681.270 K942175LINEAR TOMOGRAPHIC SYSTEM: PMT 6000

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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.