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FDA 510(k)

POINT TO POINT LEVEL

K-Number: K800761 · 1980-05-14

ApplicantRadiation Products Design, Inc.
Decision Date1980-05-14
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

POINT TO POINT LEVEL is the device name listed in this FDA 510(k) record. The listed applicant is Radiation Products Design, Inc.. It received FDA 510(k) clearance on 1980-05-14 under 510(k) number K800761. 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 POINT TO POINT LEVEL?

POINT TO POINT LEVEL is a medical device that received FDA 510(k) clearance on 1980-05-14. The listed applicant is Radiation Products Design, Inc.. The 510(k) number is K800761.

When did POINT TO POINT LEVEL receive FDA 510(k) clearance?

POINT TO POINT LEVEL received FDA 510(k) clearance on 1980-05-14, under 510(k) number K800761.

Who is the listed applicant for POINT TO POINT LEVEL?

The FDA 510(k) record lists Radiation Products Design, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POINT TO POINT LEVEL?

The FDA product code for POINT TO POINT LEVEL is IYE.

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Other records listing Radiation Products Design, Inc. 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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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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