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FDA 510(k)

SPLINT, HOAKE INFLATABLE AIR

K-Number: K781754 · 1978-11-08

ApplicantDepuy, Inc.
Decision Date1978-11-08
Product CodeKQZ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SPLINT, HOAKE INFLATABLE AIR is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1978-11-08 under 510(k) number K781754. The device is classified under product code KQZ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPLINT, HOAKE INFLATABLE AIR?

SPLINT, HOAKE INFLATABLE AIR is a medical device that received FDA 510(k) clearance on 1978-11-08. The listed applicant is Depuy, Inc.. The 510(k) number is K781754.

When did SPLINT, HOAKE INFLATABLE AIR receive FDA 510(k) clearance?

SPLINT, HOAKE INFLATABLE AIR received FDA 510(k) clearance on 1978-11-08, under 510(k) number K781754.

Who is the listed applicant for SPLINT, HOAKE INFLATABLE AIR?

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

What is the FDA product code for SPLINT, HOAKE INFLATABLE AIR?

The FDA product code for SPLINT, HOAKE INFLATABLE AIR is KQZ.

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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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