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FDA 510(k)

SAFE MATE I.V. FLUID DELIVERY SETS

K-Number: K962802 · 1996-08-28

Decision Date1996-08-28
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SAFE MATE I.V. FLUID DELIVERY SETS is the device name listed in this FDA 510(k) record. The listed applicant is Biological & Environmental Control Laboratories. It received FDA 510(k) clearance on 1996-08-28 under 510(k) number K962802. 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 SAFE MATE I.V. FLUID DELIVERY SETS?

SAFE MATE I.V. FLUID DELIVERY SETS is a medical device that received FDA 510(k) clearance on 1996-08-28. The listed applicant is Biological & Environmental Control Laboratories. The 510(k) number is K962802.

When did SAFE MATE I.V. FLUID DELIVERY SETS receive FDA 510(k) clearance?

SAFE MATE I.V. FLUID DELIVERY SETS received FDA 510(k) clearance on 1996-08-28, under 510(k) number K962802.

Who is the listed applicant for SAFE MATE I.V. FLUID DELIVERY SETS?

The FDA 510(k) record lists Biological & Environmental Control Laboratories as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SAFE MATE I.V. FLUID DELIVERY SETS?

The FDA product code for SAFE MATE I.V. FLUID DELIVERY SETS 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 Biological & Environmental Control Laboratories 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 20 devices →

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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