SCHNEIDER-SHILEY PRESSURE MANOMETER
K-Number: K861605 · 1986-05-28
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Device Summary
Frequently Asked Questions
What is the SCHNEIDER-SHILEY PRESSURE MANOMETER?
SCHNEIDER-SHILEY PRESSURE MANOMETER is a medical device that received FDA 510(k) clearance on 1986-05-28. The listed applicant is Shiley, Inc.. The 510(k) number is K861605.
When did SCHNEIDER-SHILEY PRESSURE MANOMETER receive FDA 510(k) clearance?
SCHNEIDER-SHILEY PRESSURE MANOMETER received FDA 510(k) clearance on 1986-05-28, under 510(k) number K861605.
Who is the listed applicant for SCHNEIDER-SHILEY PRESSURE MANOMETER?
The FDA 510(k) record lists Shiley, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SCHNEIDER-SHILEY PRESSURE MANOMETER?
The FDA product code for SCHNEIDER-SHILEY PRESSURE MANOMETER is KRK.
Related Clinical Trials
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.
Other records listing Shiley, Inc. as applicant
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.
Related Devices (Code: KRK)
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.
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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