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FDA 510(k)

WATERPATH SCANNING OPTION

K-Number: K781508 · 1978-09-26

ApplicantG.D. Searle and Co.
Decision Date1978-09-26
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

WATERPATH SCANNING OPTION is the device name listed in this FDA 510(k) record. The listed applicant is G.D. Searle and Co.. It received FDA 510(k) clearance on 1978-09-26 under 510(k) number K781508. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WATERPATH SCANNING OPTION?

WATERPATH SCANNING OPTION is a medical device that received FDA 510(k) clearance on 1978-09-26. The listed applicant is G.D. Searle and Co.. The 510(k) number is K781508.

When did WATERPATH SCANNING OPTION receive FDA 510(k) clearance?

WATERPATH SCANNING OPTION received FDA 510(k) clearance on 1978-09-26, under 510(k) number K781508.

Who is the listed applicant for WATERPATH SCANNING OPTION?

The FDA 510(k) record lists G.D. Searle and Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WATERPATH SCANNING OPTION?

The FDA product code for WATERPATH SCANNING OPTION is IYO.

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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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