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FDA 510(k)

MASTER-GUARD

K-Number: K884041 · 1988-10-07

ApplicantSparco, Inc.
Decision Date1988-10-07
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MASTER-GUARD is the device name listed in this FDA 510(k) record. The listed applicant is Sparco, Inc.. It received FDA 510(k) clearance on 1988-10-07 under 510(k) number K884041. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MASTER-GUARD?

MASTER-GUARD is a medical device that received FDA 510(k) clearance on 1988-10-07. The listed applicant is Sparco, Inc.. The 510(k) number is K884041.

When did MASTER-GUARD receive FDA 510(k) clearance?

MASTER-GUARD received FDA 510(k) clearance on 1988-10-07, under 510(k) number K884041.

Who is the listed applicant for MASTER-GUARD?

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

What is the FDA product code for MASTER-GUARD?

The FDA product code for MASTER-GUARD is KCT.

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Other records listing Sparco, 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.

K863964LIMB-GUARDK850268SPARCO SCOPE GUARDK850267SPARCO PIGGY-BACK POLE-INTRAVENOUS TRANSPORT POLEK844286FLASH GUARD PLASTIC VERSIONK841669FLASH GUARD

Related Devices (Code: KCT)

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.

K253988LiteSet TraysNobel Biocare ABK261935Surgical and Prosthetic TraysDentsply Sirona, Inc.K253187SteriBest® Sterilization Tray SystemMastel SurgicalK260726Straumann® ProClean™ Cassette (041.800 ; 041.801)Institut Straumann AGK252854SteriTite Container System with MediTray ProductsCase Medical, Inc.K253791PUREVUE™ Quick Connect Cannula System Tray; PUREVUE™ Quick Connect Cannula System LidDePuy Mitek, 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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