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FDA 510(k)

COMBINATION PADS STERILE SINGLES

K-Number: K802861 · 1980-12-11

ApplicantAbco Dealers, Inc.
Decision Date1980-12-11
Product CodeEFQ
DecisionSubstantially Equivalent

Device Summary

COMBINATION PADS STERILE SINGLES is the device name listed in this FDA 510(k) record. The listed applicant is Abco Dealers, Inc.. It received FDA 510(k) clearance on 1980-12-11 under 510(k) number K802861. The device is classified under product code EFQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMBINATION PADS STERILE SINGLES?

COMBINATION PADS STERILE SINGLES is a medical device that received FDA 510(k) clearance on 1980-12-11. The listed applicant is Abco Dealers, Inc.. The 510(k) number is K802861.

When did COMBINATION PADS STERILE SINGLES receive FDA 510(k) clearance?

COMBINATION PADS STERILE SINGLES received FDA 510(k) clearance on 1980-12-11, under 510(k) number K802861.

Who is the listed applicant for COMBINATION PADS STERILE SINGLES?

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

What is the FDA product code for COMBINATION PADS STERILE SINGLES?

The FDA product code for COMBINATION PADS STERILE SINGLES is EFQ.

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Other records listing Abco Dealers, Inc. as applicant

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Related Devices (Code: EFQ)

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.

K991757NON-ABSORBABLE GAUZE FOR EXTERNAL USE, STERILE AND NON STERILEFurlong IndustriesK991215SYMTEX GAUZE PADS (1'S) AND SYMTEX GAUZE SPONGES STERILE 2'S AND STERILE 10'SSymtex Healthcare Corp.K990974VITOP DRESSINGWonder & Bioenergy Hi-Tech America, Inc.K990584GAUZE SPONGES: LAPAROTOMY SPONGE, X-RAY DETECTABLEBroadline Medical IndustriesK984187CROSSTEX NON-WOVEN SPONGESCrosstex Intl.K983016GAUZE, SPONGES, CAT # 11-003Vitalcare Group, 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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