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FDA 510(k)

DEXIDE DISPOSABLE PREP STICK W/IODOPHOR

K-Number: K792270 · 1980-02-08

ApplicantDexide, Inc.
Decision Date1980-02-08
Product Code
DecisionSubstantially Equivalent

Device Summary

DEXIDE DISPOSABLE PREP STICK W/IODOPHOR is the device name listed in this FDA 510(k) record. The listed applicant is Dexide, Inc.. It received FDA 510(k) clearance on 1980-02-08 under 510(k) number K792270. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEXIDE DISPOSABLE PREP STICK W/IODOPHOR?

DEXIDE DISPOSABLE PREP STICK W/IODOPHOR is a medical device that received FDA 510(k) clearance on 1980-02-08. The listed applicant is Dexide, Inc.. The 510(k) number is K792270.

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

DEXIDE DISPOSABLE PREP STICK W/IODOPHOR received FDA 510(k) clearance on 1980-02-08, under 510(k) number K792270.

Who is the listed applicant for DEXIDE DISPOSABLE PREP STICK W/IODOPHOR?

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

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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

View all 38 devices →

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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