GRAHAM-FIELD CONDUCTIVE ECG SPRAY
K-Number: K944599 · 1996-05-07
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Device Summary
Frequently Asked Questions
What is the GRAHAM-FIELD CONDUCTIVE ECG SPRAY?
GRAHAM-FIELD CONDUCTIVE ECG SPRAY is a medical device that received FDA 510(k) clearance on 1996-05-07. The listed applicant is Chester Labs, Inc.. The 510(k) number is K944599.
When did GRAHAM-FIELD CONDUCTIVE ECG SPRAY receive FDA 510(k) clearance?
GRAHAM-FIELD CONDUCTIVE ECG SPRAY received FDA 510(k) clearance on 1996-05-07, under 510(k) number K944599.
Who is the listed applicant for GRAHAM-FIELD CONDUCTIVE ECG SPRAY?
The FDA 510(k) record lists Chester Labs, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GRAHAM-FIELD CONDUCTIVE ECG SPRAY?
The FDA product code for GRAHAM-FIELD CONDUCTIVE ECG SPRAY is GYB.
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 Chester Labs, 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: GYB)
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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