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FDA 510(k)

STERILIZATION PROCESS CHANGE BOUNDARY

K-Number: K792621 · 1980-01-11

ApplicantProcter & Gamble Mfg. Co.
Decision Date1980-01-11
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STERILIZATION PROCESS CHANGE BOUNDARY is the device name listed in this FDA 510(k) record. The listed applicant is Procter & Gamble Mfg. Co.. It received FDA 510(k) clearance on 1980-01-11 under 510(k) number K792621. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILIZATION PROCESS CHANGE BOUNDARY?

STERILIZATION PROCESS CHANGE BOUNDARY is a medical device that received FDA 510(k) clearance on 1980-01-11. The listed applicant is Procter & Gamble Mfg. Co.. The 510(k) number is K792621.

When did STERILIZATION PROCESS CHANGE BOUNDARY receive FDA 510(k) clearance?

STERILIZATION PROCESS CHANGE BOUNDARY received FDA 510(k) clearance on 1980-01-11, under 510(k) number K792621.

Who is the listed applicant for STERILIZATION PROCESS CHANGE BOUNDARY?

The FDA 510(k) record lists Procter & Gamble Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STERILIZATION PROCESS CHANGE BOUNDARY?

The FDA product code for STERILIZATION PROCESS CHANGE BOUNDARY is KKX.

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Other records listing Procter & Gamble Mfg. Co. as applicant

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Related Devices (Code: KKX)

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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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