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FDA 510(k)

PUSH CUSH

K-Number: K864108 · 1986-11-14

Decision Date1986-11-14
Product CodeKIC
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PUSH CUSH is the device name listed in this FDA 510(k) record. The listed applicant is Medical Industries America, Inc.. It received FDA 510(k) clearance on 1986-11-14 under 510(k) number K864108. The device is classified under product code KIC. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PUSH CUSH?

PUSH CUSH is a medical device that received FDA 510(k) clearance on 1986-11-14. The listed applicant is Medical Industries America, Inc.. The 510(k) number is K864108.

When did PUSH CUSH receive FDA 510(k) clearance?

PUSH CUSH received FDA 510(k) clearance on 1986-11-14, under 510(k) number K864108.

Who is the listed applicant for PUSH CUSH?

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

What is the FDA product code for PUSH CUSH?

The FDA product code for PUSH CUSH is KIC.

Other records listing Medical Industries America, 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.

View all 19 devices →

Related Devices (Code: KIC)

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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