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FDA 510(k)

PROPPER SHARPGUARD & TRAYPAD STERIL. AID

K-Number: K802428 · 1980-10-23

ApplicantPropper Mfg. Co., Inc.
Decision Date1980-10-23
Product CodeFRG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PROPPER SHARPGUARD & TRAYPAD STERIL. AID is the device name listed in this FDA 510(k) record. The listed applicant is Propper Mfg. Co., Inc.. It received FDA 510(k) clearance on 1980-10-23 under 510(k) number K802428. The device is classified under product code FRG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROPPER SHARPGUARD & TRAYPAD STERIL. AID?

PROPPER SHARPGUARD & TRAYPAD STERIL. AID is a medical device that received FDA 510(k) clearance on 1980-10-23. The listed applicant is Propper Mfg. Co., Inc.. The 510(k) number is K802428.

When did PROPPER SHARPGUARD & TRAYPAD STERIL. AID receive FDA 510(k) clearance?

PROPPER SHARPGUARD & TRAYPAD STERIL. AID received FDA 510(k) clearance on 1980-10-23, under 510(k) number K802428.

Who is the listed applicant for PROPPER SHARPGUARD & TRAYPAD STERIL. AID?

The FDA 510(k) record lists Propper Mfg. Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PROPPER SHARPGUARD & TRAYPAD STERIL. AID?

The FDA product code for PROPPER SHARPGUARD & TRAYPAD STERIL. AID is FRG.

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Other records listing Propper Mfg. Co., 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.

K111453STEAM DOT BLU PROCESS INDICATORK102894CLASSIX CHEMICAL STERILIZATION INDICATORK082620ONCE-A-DAY VERTOS TEST PACKK031152PROPPER VAPOR LINE PCD (STEAM STERILIZATION PROCESS CHALLENGE TEST)K991618BI-O.K. SELF-CONTAINED BIOLOGICAL INDICATORK991276PASS/FAIL CHALLENGE PACK

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Related Devices (Code: FRG)

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.

K261897HALYARD* ARMOR-FLEX* Sterilization Wrap with ASSURE-DRY* Technology; HALYARD* HEAVY-FLEX* Sterilization Wrap with ASSURE-DRY* Technology; HALYARD* STANDARD-FLEX* Sterilization Wrap with ASSURE-DRY* Technology; HALYARD* H300W Sterilization Wrap with ASSURE-DRY* TechnologyO&M Halyard, Inc.K252823Dukal Crepe Paper Sterilization WrapDukal, LLCK253454HALYARD* ONE-STEP* Sterilization Wrap; HALYARD* QUICK CHECK* Sterilization Wrap; HALYARD* SEQUENTIAL Sterilization Wrap; HALYARD* SMART-FOLD* Sterilization WrapO&M Halyard, Inc.K251347Sterilization Pouch/RollSterivic Medical Co., Ltd.K251177Self-Seal Sterilization Pouch and RollGuangdong Maidi Medical Co., Ltd.K250306Chex-All Sterilization Pouches and TubesPropper Manufacturing Co., 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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