Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

BRUSH/SPONGE, DISPOSABLE

K-Number: K782172 · 1979-01-10

ApplicantDexide, Inc.
Decision Date1979-01-10
Product CodeGEC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BRUSH/SPONGE, DISPOSABLE is the device name listed in this FDA 510(k) record. The listed applicant is Dexide, Inc.. It received FDA 510(k) clearance on 1979-01-10 under 510(k) number K782172. 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 BRUSH/SPONGE, DISPOSABLE?

BRUSH/SPONGE, DISPOSABLE is a medical device that received FDA 510(k) clearance on 1979-01-10. The listed applicant is Dexide, Inc.. The 510(k) number is K782172.

When did BRUSH/SPONGE, DISPOSABLE receive FDA 510(k) clearance?

BRUSH/SPONGE, DISPOSABLE received FDA 510(k) clearance on 1979-01-10, under 510(k) number K782172.

Who is the listed applicant for BRUSH/SPONGE, DISPOSABLE?

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 BRUSH/SPONGE, DISPOSABLE?

The FDA product code for BRUSH/SPONGE, DISPOSABLE is GEC.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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 →

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.

↑