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FDA 510(k)

PEACOCK PLAN

K-Number: K940663 · 1996-04-09

ApplicantNomos Corp.
Decision Date1996-04-09
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PEACOCK PLAN is the device name listed in this FDA 510(k) record. The listed applicant is Nomos Corp.. It received FDA 510(k) clearance on 1996-04-09 under 510(k) number K940663. 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 PLAN?

PEACOCK PLAN is a medical device that received FDA 510(k) clearance on 1996-04-09. The listed applicant is Nomos Corp.. The 510(k) number is K940663.

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

PEACOCK PLAN received FDA 510(k) clearance on 1996-04-09, under 510(k) number K940663.

Who is the listed applicant for PEACOCK PLAN?

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 PLAN?

The FDA product code for PEACOCK PLAN 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.

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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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