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FDA 510(k)

NOMOS SLIT COLLIMATOR (BEAK)

K-Number: K974310 · 1998-02-06

ApplicantNomos Corp.
Decision Date1998-02-06
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

NOMOS SLIT COLLIMATOR (BEAK) is the device name listed in this FDA 510(k) record. The listed applicant is Nomos Corp.. It received FDA 510(k) clearance on 1998-02-06 under 510(k) number K974310. 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 NOMOS SLIT COLLIMATOR (BEAK)?

NOMOS SLIT COLLIMATOR (BEAK) is a medical device that received FDA 510(k) clearance on 1998-02-06. The listed applicant is Nomos Corp.. The 510(k) number is K974310.

When did NOMOS SLIT COLLIMATOR (BEAK) receive FDA 510(k) clearance?

NOMOS SLIT COLLIMATOR (BEAK) received FDA 510(k) clearance on 1998-02-06, under 510(k) number K974310.

Who is the listed applicant for NOMOS SLIT COLLIMATOR (BEAK)?

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 NOMOS SLIT COLLIMATOR (BEAK)?

The FDA product code for NOMOS SLIT COLLIMATOR (BEAK) 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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