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FDA 510(k)

DISPOSABLE FLUSH DEVICE

K-Number: K860681 · 1986-06-17

ApplicantHewlett-Packard Co.
Decision Date1986-06-17
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE FLUSH DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Hewlett-Packard Co.. It received FDA 510(k) clearance on 1986-06-17 under 510(k) number K860681. The device is classified under product code DRS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE FLUSH DEVICE?

DISPOSABLE FLUSH DEVICE is a medical device that received FDA 510(k) clearance on 1986-06-17. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K860681.

When did DISPOSABLE FLUSH DEVICE receive FDA 510(k) clearance?

DISPOSABLE FLUSH DEVICE received FDA 510(k) clearance on 1986-06-17, under 510(k) number K860681.

Who is the listed applicant for DISPOSABLE FLUSH DEVICE?

The FDA 510(k) record lists Hewlett-Packard Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOSABLE FLUSH DEVICE?

The FDA product code for DISPOSABLE FLUSH DEVICE is DRS.

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Other records listing Hewlett-Packard Co. as applicant

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Related Devices (Code: DRS)

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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