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FDA 510(k)

TRAY, BLOOD SAMPLING (PULSATOR II)

K-Number: K760086 · 1976-07-16

Decision Date1976-07-16
Product CodeGJE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TRAY, BLOOD SAMPLING (PULSATOR II) is the device name listed in this FDA 510(k) record. The listed applicant is Concord Laboratories, Inc.. It received FDA 510(k) clearance on 1976-07-16 under 510(k) number K760086. The device is classified under product code GJE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 42 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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