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FDA 510(k)

STERILIZATION PROCESS/T-BINDER

K-Number: K792629 · 1980-01-11

ApplicantProcter & Gamble Mfg. Co.
Decision Date1980-01-11
Product CodeKMO
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERILIZATION PROCESS/T-BINDER 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 K792629. The device is classified under product code KMO. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILIZATION PROCESS/T-BINDER?

STERILIZATION PROCESS/T-BINDER 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 K792629.

When did STERILIZATION PROCESS/T-BINDER receive FDA 510(k) clearance?

STERILIZATION PROCESS/T-BINDER received FDA 510(k) clearance on 1980-01-11, under 510(k) number K792629.

Who is the listed applicant for STERILIZATION PROCESS/T-BINDER?

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/T-BINDER?

The FDA product code for STERILIZATION PROCESS/T-BINDER is KMO.

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Other records listing Procter & Gamble Mfg. Co. 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.

K873457SCENTED OR SCENTED DEODORIZED MENSTRUAL PADSK873036ATTENDS INCONTINENT BRIEFK864673UNSCENTED MENSTRUAL PADK861863MODIFIED PROTECTIVE GARMENTK862348SINGLE-USE PATIENT UNDERPADK860598MODIFIED PROTECTIVE GARMENT FOR INCONTINENTS

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Related Devices (Code: KMO)

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.

K9218524 SURE TM RECTAL TUBEBoston Pacific Medical, Inc.K893809COUGH PILLOWCustom Hospitals ProductsK883214THORACIC SUPPORT SYSTEMStorer Medical ProductsK882592HEART HUGGER STERNUM SUPPORT HARNESSGeneral Cardiac Technology, Inc.

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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