TRAY, BLOOD SAMPLING (PULSATOR II)
K-Number: K760086 · 1976-07-16
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Device Summary
Frequently Asked Questions
What is the TRAY, BLOOD SAMPLING (PULSATOR II)?
TRAY, BLOOD SAMPLING (PULSATOR II) is a medical device that received FDA 510(k) clearance on 1976-07-16. The listed applicant is Concord Laboratories, Inc.. The 510(k) number is K760086.
When did TRAY, BLOOD SAMPLING (PULSATOR II) receive FDA 510(k) clearance?
TRAY, BLOOD SAMPLING (PULSATOR II) received FDA 510(k) clearance on 1976-07-16, under 510(k) number K760086.
Who is the listed applicant for TRAY, BLOOD SAMPLING (PULSATOR II)?
The FDA 510(k) record lists Concord Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TRAY, BLOOD SAMPLING (PULSATOR II)?
The FDA product code for TRAY, BLOOD SAMPLING (PULSATOR II) is GJE.
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 Concord Laboratories, 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: GJE)
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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