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FDA 510(k)

AB2 MED-FLO SOLUTION SET

K-Number: K984569 · 1999-08-12

ApplicantAb2 Medical Products, Llp
Decision Date1999-08-12
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AB2 MED-FLO SOLUTION SET is the device name listed in this FDA 510(k) record. The listed applicant is Ab2 Medical Products, Llp. It received FDA 510(k) clearance on 1999-08-12 under 510(k) number K984569. 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 AB2 MED-FLO SOLUTION SET?

AB2 MED-FLO SOLUTION SET is a medical device that received FDA 510(k) clearance on 1999-08-12. The listed applicant is Ab2 Medical Products, Llp. The 510(k) number is K984569.

When did AB2 MED-FLO SOLUTION SET receive FDA 510(k) clearance?

AB2 MED-FLO SOLUTION SET received FDA 510(k) clearance on 1999-08-12, under 510(k) number K984569.

Who is the listed applicant for AB2 MED-FLO SOLUTION SET?

The FDA 510(k) record lists Ab2 Medical Products, Llp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AB2 MED-FLO SOLUTION SET?

The FDA product code for AB2 MED-FLO SOLUTION SET is FPA.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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