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FDA 510(k)

I.V. SETS WALRUS BRAND VARIOUS CONFIGUR-

K-Number: K830755 · 1983-04-28

Decision Date1983-04-28
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

I.V. SETS WALRUS BRAND VARIOUS CONFIGUR- is the device name listed in this FDA 510(k) record. The listed applicant is Medical Parameters, Inc.. It received FDA 510(k) clearance on 1983-04-28 under 510(k) number K830755. 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 I.V. SETS WALRUS BRAND VARIOUS CONFIGUR-?

I.V. SETS WALRUS BRAND VARIOUS CONFIGUR- is a medical device that received FDA 510(k) clearance on 1983-04-28. The listed applicant is Medical Parameters, Inc.. The 510(k) number is K830755.

When did I.V. SETS WALRUS BRAND VARIOUS CONFIGUR- receive FDA 510(k) clearance?

I.V. SETS WALRUS BRAND VARIOUS CONFIGUR- received FDA 510(k) clearance on 1983-04-28, under 510(k) number K830755.

Who is the listed applicant for I.V. SETS WALRUS BRAND VARIOUS CONFIGUR-?

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

What is the FDA product code for I.V. SETS WALRUS BRAND VARIOUS CONFIGUR-?

The FDA product code for I.V. SETS WALRUS BRAND VARIOUS CONFIGUR- 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 Medical Parameters, 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: 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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