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FDA 510(k)

N.E.W. NEB

K-Number: K830527 · 1983-04-12

ApplicantSan Diego Plastics, Inc.
Decision Date1983-04-12
Product Code
DecisionSubstantially Equivalent

Device Summary

N.E.W. NEB is the device name listed in this FDA 510(k) record. The listed applicant is San Diego Plastics, Inc.. It received FDA 510(k) clearance on 1983-04-12 under 510(k) number K830527. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the N.E.W. NEB?

N.E.W. NEB is a medical device that received FDA 510(k) clearance on 1983-04-12. The listed applicant is San Diego Plastics, Inc.. The 510(k) number is K830527.

When did N.E.W. NEB receive FDA 510(k) clearance?

N.E.W. NEB received FDA 510(k) clearance on 1983-04-12, under 510(k) number K830527.

Who is the listed applicant for N.E.W. NEB?

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

Other records listing San Diego Plastics, 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.

K832660OXYGEN CONNECTING TUBESET-RESPIRATORY

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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