FDA 510(k)

STA-PUT

K-Number: K872358 · 1987-08-06

Decision Date1987-08-06

Product CodeKMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

STA-PUT is the device name listed in this FDA 510(k) record. The listed applicant is Design Technologies, Inc.. It received FDA 510(k) clearance on 1987-08-06 under 510(k) number K872358. The device is classified under product code KMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STA-PUT?

STA-PUT is a medical device that received FDA 510(k) clearance on 1987-08-06. The listed applicant is Design Technologies, Inc.. The 510(k) number is K872358.

When did STA-PUT receive FDA 510(k) clearance?

STA-PUT received FDA 510(k) clearance on 1987-08-06, under 510(k) number K872358.

Who is the listed applicant for STA-PUT?

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

What is the FDA product code for STA-PUT?

The FDA product code for STA-PUT is KMI.

Other records listing Design Technologies, 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.

K872038NEB-U-VENT K871262MODIFIED NOFLO I K863613NO-FLO I

Related Devices (Code: KMI)

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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.