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FDA 510(k)

ADAC XL-PLAN-PC

K-Number: K920041 · 1992-03-30

ApplicantAdac Laboratories
Decision Date1992-03-30
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ADAC XL-PLAN-PC is the device name listed in this FDA 510(k) record. The listed applicant is Adac Laboratories. It received FDA 510(k) clearance on 1992-03-30 under 510(k) number K920041. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADAC XL-PLAN-PC?

ADAC XL-PLAN-PC is a medical device that received FDA 510(k) clearance on 1992-03-30. The listed applicant is Adac Laboratories. The 510(k) number is K920041.

When did ADAC XL-PLAN-PC receive FDA 510(k) clearance?

ADAC XL-PLAN-PC received FDA 510(k) clearance on 1992-03-30, under 510(k) number K920041.

Who is the listed applicant for ADAC XL-PLAN-PC?

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

What is the FDA product code for ADAC XL-PLAN-PC?

The FDA product code for ADAC XL-PLAN-PC is IYE.

Other records listing Adac 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.

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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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