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FDA 510(k)

MASTER MEDICAL DEVICE IS I.V. STAT 2

K-Number: K871753 · 1987-06-05

Decision Date1987-06-05
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MASTER MEDICAL DEVICE IS I.V. STAT 2 is the device name listed in this FDA 510(k) record. The listed applicant is The Master Medical Corp.. It received FDA 510(k) clearance on 1987-06-05 under 510(k) number K871753. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MASTER MEDICAL DEVICE IS I.V. STAT 2?

MASTER MEDICAL DEVICE IS I.V. STAT 2 is a medical device that received FDA 510(k) clearance on 1987-06-05. The listed applicant is The Master Medical Corp.. The 510(k) number is K871753.

When did MASTER MEDICAL DEVICE IS I.V. STAT 2 receive FDA 510(k) clearance?

MASTER MEDICAL DEVICE IS I.V. STAT 2 received FDA 510(k) clearance on 1987-06-05, under 510(k) number K871753.

Who is the listed applicant for MASTER MEDICAL DEVICE IS I.V. STAT 2?

The FDA 510(k) record lists The Master Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MASTER MEDICAL DEVICE IS I.V. STAT 2?

The FDA product code for MASTER MEDICAL DEVICE IS I.V. STAT 2 is FPA.

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 The Master Medical Corp. 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: FPA)

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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