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FDA 510(k)

DECUB-I-CON 800 AND 900 SYSTEM

K-Number: K871614 · 1987-08-21

Decision Date1987-08-21
Product CodeIOQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

DECUB-I-CON 800 AND 900 SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Wholesale Medical Supply, Inc.. It received FDA 510(k) clearance on 1987-08-21 under 510(k) number K871614. The device is classified under product code IOQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DECUB-I-CON 800 AND 900 SYSTEM?

DECUB-I-CON 800 AND 900 SYSTEM is a medical device that received FDA 510(k) clearance on 1987-08-21. The listed applicant is Wholesale Medical Supply, Inc.. The 510(k) number is K871614.

When did DECUB-I-CON 800 AND 900 SYSTEM receive FDA 510(k) clearance?

DECUB-I-CON 800 AND 900 SYSTEM received FDA 510(k) clearance on 1987-08-21, under 510(k) number K871614.

Who is the listed applicant for DECUB-I-CON 800 AND 900 SYSTEM?

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

What is the FDA product code for DECUB-I-CON 800 AND 900 SYSTEM?

The FDA product code for DECUB-I-CON 800 AND 900 SYSTEM is IOQ.

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: IOQ)

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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