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FDA 510(k)

STERILE ADHERENT DRAPES

K-Number: K812809 · 1981-11-06

ApplicantAbco Dealers, Inc.
Decision Date1981-11-06
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STERILE ADHERENT DRAPES 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 1981-11-06 under 510(k) number K812809. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE ADHERENT DRAPES?

STERILE ADHERENT DRAPES is a medical device that received FDA 510(k) clearance on 1981-11-06. The listed applicant is Abco Dealers, Inc.. The 510(k) number is K812809.

When did STERILE ADHERENT DRAPES receive FDA 510(k) clearance?

STERILE ADHERENT DRAPES received FDA 510(k) clearance on 1981-11-06, under 510(k) number K812809.

Who is the listed applicant for STERILE ADHERENT DRAPES?

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 STERILE ADHERENT DRAPES?

The FDA product code for STERILE ADHERENT DRAPES is KKX.

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Other records listing Abco Dealers, 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.

K905025DIGITAL THERMOMETER KITSK882304DIGITAL THERMOMETER SHEATHS (ORAL AND RECTAL)K880892BLOOD COLLECTING NEEDLE AND HOLDERSK880894ALLERGIST SYRINGESK872875STRETCH GAUZE BANDAGESK872874MICROSCOPE COVER GLASSES

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Related Devices (Code: KKX)

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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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