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FDA 510(k)

MNITROL HEMOTOL. REF. AND CONTROL

K-Number: K770384 · 1977-04-08

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1977-04-08
Product CodeJPK
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

MNITROL HEMOTOL. REF. AND CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. It received FDA 510(k) clearance on 1977-04-08 under 510(k) number K770384. The device is classified under product code JPK. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MNITROL HEMOTOL. REF. AND CONTROL?

MNITROL HEMOTOL. REF. AND CONTROL is a medical device that received FDA 510(k) clearance on 1977-04-08. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K770384.

When did MNITROL HEMOTOL. REF. AND CONTROL receive FDA 510(k) clearance?

MNITROL HEMOTOL. REF. AND CONTROL received FDA 510(k) clearance on 1977-04-08, under 510(k) number K770384.

Who is the listed applicant for MNITROL HEMOTOL. REF. AND CONTROL?

The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MNITROL HEMOTOL. REF. AND CONTROL?

The FDA product code for MNITROL HEMOTOL. REF. AND CONTROL is JPK.

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Related Devices (Code: JPK)

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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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