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FDA 510(k)

MODIFIED ICT/B INTRACRANIAL PRESS. TRANS. EPIDURAL

K-Number: K863479 · 1986-10-14

ApplicantMedical Measurements, Inc.
Decision Date1986-10-14
Product CodeGWM
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MODIFIED ICT/B INTRACRANIAL PRESS. TRANS. EPIDURAL is the device name listed in this FDA 510(k) record. The listed applicant is Medical Measurements, Inc.. It received FDA 510(k) clearance on 1986-10-14 under 510(k) number K863479. 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 MODIFIED ICT/B INTRACRANIAL PRESS. TRANS. EPIDURAL?

MODIFIED ICT/B INTRACRANIAL PRESS. TRANS. EPIDURAL is a medical device that received FDA 510(k) clearance on 1986-10-14. The listed applicant is Medical Measurements, Inc.. The 510(k) number is K863479.

When did MODIFIED ICT/B INTRACRANIAL PRESS. TRANS. EPIDURAL receive FDA 510(k) clearance?

MODIFIED ICT/B INTRACRANIAL PRESS. TRANS. EPIDURAL received FDA 510(k) clearance on 1986-10-14, under 510(k) number K863479.

Who is the listed applicant for MODIFIED ICT/B INTRACRANIAL PRESS. TRANS. EPIDURAL?

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

What is the FDA product code for MODIFIED ICT/B INTRACRANIAL PRESS. TRANS. EPIDURAL?

The FDA product code for MODIFIED ICT/B INTRACRANIAL PRESS. TRANS. EPIDURAL is GWM.

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Related Devices (Code: GWM)

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.

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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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