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FDA 510(k)

JOSTRA HL-20 TWIN PUMP

K-Number: K984338 · 1999-08-19

ApplicantJostra Bentley
Decision Date1999-08-19
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

JOSTRA HL-20 TWIN PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Jostra Bentley. It received FDA 510(k) clearance on 1999-08-19 under 510(k) number K984338. The device is classified under product code DPW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JOSTRA HL-20 TWIN PUMP?

JOSTRA HL-20 TWIN PUMP is a medical device that received FDA 510(k) clearance on 1999-08-19. The listed applicant is Jostra Bentley. The 510(k) number is K984338.

When did JOSTRA HL-20 TWIN PUMP receive FDA 510(k) clearance?

JOSTRA HL-20 TWIN PUMP received FDA 510(k) clearance on 1999-08-19, under 510(k) number K984338.

Who is the listed applicant for JOSTRA HL-20 TWIN PUMP?

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

What is the FDA product code for JOSTRA HL-20 TWIN PUMP?

The FDA product code for JOSTRA HL-20 TWIN PUMP is DPW.

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Other records listing Jostra Bentley 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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Related Devices (Code: DPW)

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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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