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FDA 510(k)

SILICONE BRAIN SPATULA SET

K-Number: K923723 · 1992-08-12

ApplicantRedmond Neurosurgical, Inc.
Decision Date1992-08-12
Product CodeHAO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

SILICONE BRAIN SPATULA SET is the device name listed in this FDA 510(k) record. The listed applicant is Redmond Neurosurgical, Inc.. It received FDA 510(k) clearance on 1992-08-12 under 510(k) number K923723. The device is classified under product code HAO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SILICONE BRAIN SPATULA SET?

SILICONE BRAIN SPATULA SET is a medical device that received FDA 510(k) clearance on 1992-08-12. The listed applicant is Redmond Neurosurgical, Inc.. The 510(k) number is K923723.

When did SILICONE BRAIN SPATULA SET receive FDA 510(k) clearance?

SILICONE BRAIN SPATULA SET received FDA 510(k) clearance on 1992-08-12, under 510(k) number K923723.

Who is the listed applicant for SILICONE BRAIN SPATULA SET?

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

What is the FDA product code for SILICONE BRAIN SPATULA SET?

The FDA product code for SILICONE BRAIN SPATULA SET is HAO.

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Related Devices (Code: HAO)

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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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