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FDA 510(k)

CUSHMAN MANUFACTURING, INC. ULTRA 6.0.

K-Number: K960802 · 1996-06-18

ApplicantCushman Mfg., Inc.
Decision Date1996-06-18
Product CodeIMI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CUSHMAN MANUFACTURING, INC. ULTRA 6.0. is the device name listed in this FDA 510(k) record. The listed applicant is Cushman Mfg., Inc.. It received FDA 510(k) clearance on 1996-06-18 under 510(k) number K960802. The device is classified under product code IMI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CUSHMAN MANUFACTURING, INC. ULTRA 6.0.?

CUSHMAN MANUFACTURING, INC. ULTRA 6.0. is a medical device that received FDA 510(k) clearance on 1996-06-18. The listed applicant is Cushman Mfg., Inc.. The 510(k) number is K960802.

When did CUSHMAN MANUFACTURING, INC. ULTRA 6.0. receive FDA 510(k) clearance?

CUSHMAN MANUFACTURING, INC. ULTRA 6.0. received FDA 510(k) clearance on 1996-06-18, under 510(k) number K960802.

Who is the listed applicant for CUSHMAN MANUFACTURING, INC. ULTRA 6.0.?

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

What is the FDA product code for CUSHMAN MANUFACTURING, INC. ULTRA 6.0.?

The FDA product code for CUSHMAN MANUFACTURING, INC. ULTRA 6.0. is IMI.

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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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