E100A PULSE OXIMETER FINGER SENSOR/PROBE
K-Number: K954168 · 1996-09-12
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Device Summary
Frequently Asked Questions
What is the E100A PULSE OXIMETER FINGER SENSOR/PROBE?
E100A PULSE OXIMETER FINGER SENSOR/PROBE is a medical device that received FDA 510(k) clearance on 1996-09-12. The listed applicant is Epic Medical Equipment Services, Inc.. The 510(k) number is K954168.
When did E100A PULSE OXIMETER FINGER SENSOR/PROBE receive FDA 510(k) clearance?
E100A PULSE OXIMETER FINGER SENSOR/PROBE received FDA 510(k) clearance on 1996-09-12, under 510(k) number K954168.
Who is the listed applicant for E100A PULSE OXIMETER FINGER SENSOR/PROBE?
The FDA 510(k) record lists Epic Medical Equipment Services, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for E100A PULSE OXIMETER FINGER SENSOR/PROBE?
The FDA product code for E100A PULSE OXIMETER FINGER SENSOR/PROBE is DQA.
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 Epic Medical Equipment Services, 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: DQA)
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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