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FDA 510(k)

PLAN A LIFE

K-Number: K830975 · 1983-05-04

ApplicantNew Directions Co.
Decision Date1983-05-04
Product CodeJIN
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PLAN A LIFE is the device name listed in this FDA 510(k) record. The listed applicant is New Directions Co.. It received FDA 510(k) clearance on 1983-05-04 under 510(k) number K830975. The device is classified under product code JIN. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLAN A LIFE?

PLAN A LIFE is a medical device that received FDA 510(k) clearance on 1983-05-04. The listed applicant is New Directions Co.. The 510(k) number is K830975.

When did PLAN A LIFE receive FDA 510(k) clearance?

PLAN A LIFE received FDA 510(k) clearance on 1983-05-04, under 510(k) number K830975.

Who is the listed applicant for PLAN A LIFE?

The FDA 510(k) record lists New Directions Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PLAN A LIFE?

The FDA product code for PLAN A LIFE is JIN.

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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.

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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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