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FDA 510(k)

STERILIZATION PROCESS/X-RAY DETECT. SPG

K-Number: K792630 · 1980-01-11

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

Device Summary

STERILIZATION PROCESS/X-RAY DETECT. SPG 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 K792630. The device is classified under product code GDY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILIZATION PROCESS/X-RAY DETECT. SPG?

STERILIZATION PROCESS/X-RAY DETECT. SPG 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 K792630.

When did STERILIZATION PROCESS/X-RAY DETECT. SPG receive FDA 510(k) clearance?

STERILIZATION PROCESS/X-RAY DETECT. SPG received FDA 510(k) clearance on 1980-01-11, under 510(k) number K792630.

Who is the listed applicant for STERILIZATION PROCESS/X-RAY DETECT. SPG?

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/X-RAY DETECT. SPG?

The FDA product code for STERILIZATION PROCESS/X-RAY DETECT. SPG is GDY.

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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: GDY)

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.

K972634ULTRACELL SUCTION SPONGEUltracell Medical Technologies, Inc.K960236CPR LAP SPONGESCustom Pack ReliabilityK955599STRYKER FEMORAL CANAL SPONGE & ACETABULUM SPONGEStryker Corp.K955322PROTEC X-RAY DETECTABLE GAUZE SPONGEDerivados DE Gasa, S.A. DE C.V.K953830KENSORBKentron Health Care, Inc.K953059KITTNER DISSECTORMedical Perspectives Corp.

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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