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FDA 510(k)

ACACIA PISTON SYRINGE

K-Number: K092986 · 2009-10-27

ApplicantAcacia, Inc.
Decision Date2009-10-27
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ACACIA PISTON SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Acacia, Inc.. It received FDA 510(k) clearance on 2009-10-27 under 510(k) number K092986. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACACIA PISTON SYRINGE?

ACACIA PISTON SYRINGE is a medical device that received FDA 510(k) clearance on 2009-10-27. The listed applicant is Acacia, Inc.. The 510(k) number is K092986.

When did ACACIA PISTON SYRINGE receive FDA 510(k) clearance?

ACACIA PISTON SYRINGE received FDA 510(k) clearance on 2009-10-27, under 510(k) number K092986.

Who is the listed applicant for ACACIA PISTON SYRINGE?

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

What is the FDA product code for ACACIA PISTON SYRINGE?

The FDA product code for ACACIA PISTON SYRINGE is FMF.

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Other records listing Acacia, 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.

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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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