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FDA 510(k)

NON-INVASIVE TUBING

K-Number: K921450 · 1993-02-05

Decision Date1993-02-05
Product CodeFPK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NON-INVASIVE TUBING is the device name listed in this FDA 510(k) record. The listed applicant is Specialty Medical Sales, Inc.. It received FDA 510(k) clearance on 1993-02-05 under 510(k) number K921450. The device is classified under product code FPK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NON-INVASIVE TUBING?

NON-INVASIVE TUBING is a medical device that received FDA 510(k) clearance on 1993-02-05. The listed applicant is Specialty Medical Sales, Inc.. The 510(k) number is K921450.

When did NON-INVASIVE TUBING receive FDA 510(k) clearance?

NON-INVASIVE TUBING received FDA 510(k) clearance on 1993-02-05, under 510(k) number K921450.

Who is the listed applicant for NON-INVASIVE TUBING?

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

What is the FDA product code for NON-INVASIVE TUBING?

The FDA product code for NON-INVASIVE TUBING is FPK.

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.

Related Devices (Code: FPK)

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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