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FDA 510(k)

STERILE IV SET 4 SIZES

K-Number: K832329 · 1983-08-24

ApplicantAbco Dealers, Inc.
Decision Date1983-08-24
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERILE IV SET 4 SIZES 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 1983-08-24 under 510(k) number K832329. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE IV SET 4 SIZES?

STERILE IV SET 4 SIZES is a medical device that received FDA 510(k) clearance on 1983-08-24. The listed applicant is Abco Dealers, Inc.. The 510(k) number is K832329.

When did STERILE IV SET 4 SIZES receive FDA 510(k) clearance?

STERILE IV SET 4 SIZES received FDA 510(k) clearance on 1983-08-24, under 510(k) number K832329.

Who is the listed applicant for STERILE IV SET 4 SIZES?

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 IV SET 4 SIZES?

The FDA product code for STERILE IV SET 4 SIZES is FPA.

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Other records listing Abco Dealers, Inc. as applicant

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Related Devices (Code: FPA)

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.

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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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