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FDA 510(k)

DEXIDE DIS. PREP SPONGE W/IDEX PATIENT P

K-Number: K792273 · 1979-12-10

ApplicantDexide, Inc.
Decision Date1979-12-10
Product CodeGEC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DEXIDE DIS. PREP SPONGE W/IDEX PATIENT P is the device name listed in this FDA 510(k) record. The listed applicant is Dexide, Inc.. It received FDA 510(k) clearance on 1979-12-10 under 510(k) number K792273. The device is classified under product code GEC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEXIDE DIS. PREP SPONGE W/IDEX PATIENT P?

DEXIDE DIS. PREP SPONGE W/IDEX PATIENT P is a medical device that received FDA 510(k) clearance on 1979-12-10. The listed applicant is Dexide, Inc.. The 510(k) number is K792273.

When did DEXIDE DIS. PREP SPONGE W/IDEX PATIENT P receive FDA 510(k) clearance?

DEXIDE DIS. PREP SPONGE W/IDEX PATIENT P received FDA 510(k) clearance on 1979-12-10, under 510(k) number K792273.

Who is the listed applicant for DEXIDE DIS. PREP SPONGE W/IDEX PATIENT P?

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 DIS. PREP SPONGE W/IDEX PATIENT P?

The FDA product code for DEXIDE DIS. PREP SPONGE W/IDEX PATIENT P is GEC.

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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: GEC)

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.

K971473IVALON INSTRUMENT WIPE, IVALON KNIFE CLEANING BLOCKM-Pact Worldwide Management Corp.K960621EXPANDACELL INSTRUMENT WIPEShippert Medical Technologies Corp.K900691BIODYNE INSTRUMENT WIPESBio-Dyne, Inc.K896085SURGI-BRUSHSparta Surgical Corp.K875033STERILE SCRUBBY SCRUB BRUSHMedsurg Industries, Inc.K875129STERI-CLENSAbsorbent Cotton 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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