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FDA 510(k)

STERILE DISPOSABLE SUCTION TUBE CATHETER

K-Number: K861923 · 1986-05-30

ApplicantPilling Co.
Decision Date1986-05-30
Product Code
DecisionSubstantially Equivalent

Device Summary

STERILE DISPOSABLE SUCTION TUBE CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Pilling Co.. It received FDA 510(k) clearance on 1986-05-30 under 510(k) number K861923. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE DISPOSABLE SUCTION TUBE CATHETER?

STERILE DISPOSABLE SUCTION TUBE CATHETER is a medical device that received FDA 510(k) clearance on 1986-05-30. The listed applicant is Pilling Co.. The 510(k) number is K861923.

When did STERILE DISPOSABLE SUCTION TUBE CATHETER receive FDA 510(k) clearance?

STERILE DISPOSABLE SUCTION TUBE CATHETER received FDA 510(k) clearance on 1986-05-30, under 510(k) number K861923.

Who is the listed applicant for STERILE DISPOSABLE SUCTION TUBE CATHETER?

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

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 Pilling Co. 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

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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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