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FDA 510(k)

AESCULAP SPIEGELBERG BRAIN PRESSURE MONITOR

K-Number: K003759 · 2001-06-28

ApplicantAesculap, Inc.
Decision Date2001-06-28
Product CodeGWM
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

AESCULAP SPIEGELBERG BRAIN PRESSURE MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 2001-06-28 under 510(k) number K003759. The device is classified under product code GWM. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AESCULAP SPIEGELBERG BRAIN PRESSURE MONITOR?

AESCULAP SPIEGELBERG BRAIN PRESSURE MONITOR is a medical device that received FDA 510(k) clearance on 2001-06-28. The listed applicant is Aesculap, Inc.. The 510(k) number is K003759.

When did AESCULAP SPIEGELBERG BRAIN PRESSURE MONITOR receive FDA 510(k) clearance?

AESCULAP SPIEGELBERG BRAIN PRESSURE MONITOR received FDA 510(k) clearance on 2001-06-28, under 510(k) number K003759.

Who is the listed applicant for AESCULAP SPIEGELBERG BRAIN PRESSURE MONITOR?

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

What is the FDA product code for AESCULAP SPIEGELBERG BRAIN PRESSURE MONITOR?

The FDA product code for AESCULAP SPIEGELBERG BRAIN PRESSURE MONITOR is GWM.

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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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