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FDA 510(k)

HD CRYSTALINE SUCTION TIP

K-Number: K860927 · 1986-03-27

Decision Date1986-03-27
Product CodeJOL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HD CRYSTALINE SUCTION TIP is the device name listed in this FDA 510(k) record. The listed applicant is Hospital Disposables, Inc.. It received FDA 510(k) clearance on 1986-03-27 under 510(k) number K860927. The device is classified under product code JOL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HD CRYSTALINE SUCTION TIP?

HD CRYSTALINE SUCTION TIP is a medical device that received FDA 510(k) clearance on 1986-03-27. The listed applicant is Hospital Disposables, Inc.. The 510(k) number is K860927.

When did HD CRYSTALINE SUCTION TIP receive FDA 510(k) clearance?

HD CRYSTALINE SUCTION TIP received FDA 510(k) clearance on 1986-03-27, under 510(k) number K860927.

Who is the listed applicant for HD CRYSTALINE SUCTION TIP?

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

What is the FDA product code for HD CRYSTALINE SUCTION TIP?

The FDA product code for HD CRYSTALINE SUCTION TIP is JOL.

Related Clinical Trials

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.

Other records listing Hospital Disposables, 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.

Related Devices (Code: JOL)

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.

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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