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FDA 510(k)

PEACOCK SYSTEM

K-Number: K963258 · 1996-11-18

ApplicantNomos Corp.
Decision Date1996-11-18
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PEACOCK SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Nomos Corp.. It received FDA 510(k) clearance on 1996-11-18 under 510(k) number K963258. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEACOCK SYSTEM?

PEACOCK SYSTEM is a medical device that received FDA 510(k) clearance on 1996-11-18. The listed applicant is Nomos Corp.. The 510(k) number is K963258.

When did PEACOCK SYSTEM receive FDA 510(k) clearance?

PEACOCK SYSTEM received FDA 510(k) clearance on 1996-11-18, under 510(k) number K963258.

Who is the listed applicant for PEACOCK SYSTEM?

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

What is the FDA product code for PEACOCK SYSTEM?

The FDA product code for PEACOCK SYSTEM is IYE.

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Other records listing Nomos 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.

K070611BAT ULTRASOUND LOCALIZATION AND POSITIONING SYSTEM, VERSION 6K060895NOMOSSTAT, VERSION 1.0K042875NAVIGATORK032209NOMOS CORVUS 5.0MK013036NOMOS MOTORIZED CRANE IIK993675PEREGRINE RADIATION THERAPY DOSE CALCULATION SYSTEM

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Related Devices (Code: IYE)

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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.

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