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FDA 510(k)

HI VOLUME PUMPING CHAMBER

K-Number: K802561 · 1980-10-31

ApplicantAcacia, Inc.
Decision Date1980-10-31
Product CodeJTB
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

HI VOLUME PUMPING CHAMBER is the device name listed in this FDA 510(k) record. The listed applicant is Acacia, Inc.. It received FDA 510(k) clearance on 1980-10-31 under 510(k) number K802561. The device is classified under product code JTB. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HI VOLUME PUMPING CHAMBER?

HI VOLUME PUMPING CHAMBER is a medical device that received FDA 510(k) clearance on 1980-10-31. The listed applicant is Acacia, Inc.. The 510(k) number is K802561.

When did HI VOLUME PUMPING CHAMBER receive FDA 510(k) clearance?

HI VOLUME PUMPING CHAMBER received FDA 510(k) clearance on 1980-10-31, under 510(k) number K802561.

Who is the listed applicant for HI VOLUME PUMPING CHAMBER?

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 HI VOLUME PUMPING CHAMBER?

The FDA product code for HI VOLUME PUMPING CHAMBER is JTB.

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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.

K122449ENTERAL NUTRITION WARMERK111381MEDI-SIS SYRINGE INFUSION SYSTEMK103165BLOOD SAMPLING SETK092986ACACIA PISTON SYRINGEK972538FLOW-EZE BLUNT CANNULA (1999BC)K931095SPRING LOADED SYRINGE

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Related Devices (Code: JTB)

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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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