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FDA 510(k)

DEXIDE DISPOSABLE PREP STICK

K-Number: K791168 · 1979-07-30

ApplicantDexide, Inc.
Decision Date1979-07-30
Product CodeKXF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DEXIDE DISPOSABLE PREP STICK is the device name listed in this FDA 510(k) record. The listed applicant is Dexide, Inc.. It received FDA 510(k) clearance on 1979-07-30 under 510(k) number K791168. The device is classified under product code KXF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEXIDE DISPOSABLE PREP STICK?

DEXIDE DISPOSABLE PREP STICK is a medical device that received FDA 510(k) clearance on 1979-07-30. The listed applicant is Dexide, Inc.. The 510(k) number is K791168.

When did DEXIDE DISPOSABLE PREP STICK receive FDA 510(k) clearance?

DEXIDE DISPOSABLE PREP STICK received FDA 510(k) clearance on 1979-07-30, under 510(k) number K791168.

Who is the listed applicant for DEXIDE DISPOSABLE PREP STICK?

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

What is the FDA product code for DEXIDE DISPOSABLE PREP STICK?

The FDA product code for DEXIDE DISPOSABLE PREP STICK is KXF.

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Other records listing Dexide, 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.

K991814MULTACHOICE INSTRUMENTSK990379MODIFICATION TO MULTAPORT CANNULA, REDUCER AND ACCESSORIESK981940MULTAPUMP DISPOSABLE PUMP HEAD AND ACCESSORIESK981941MULTAPORT CANNULA REDUCER AND ACCESSORIESK953611DEXIDE ENDO-LUBE KITK944509DEXIDE INSUFFLATION TUBING WITH FILTER

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Related Devices (Code: KXF)

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.

K123184FINN CHAMBERS AQUASmartpracticeK103409ALLERGEAZE R CLEARSmartpracticeK063160ALLERGEAZE PATCH TEST CHAMBERSSmartpracticeK013820FINN CHAMBER (R)Epitest Ltd. OYK992553IQ CHAMBERSDormer Laboratories, Inc.K870762EAR APPLICATOR, CATALOG NO. 2229Treace Medical, 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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