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FDA 510(k)

ID-ZONE LD ISOENZYME CONTROL

K-Number: K822984 · 1982-11-10

ApplicantBeckman Instruments, Inc.
Decision Date1982-11-10
Product CodeJJT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ID-ZONE LD ISOENZYME CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Beckman Instruments, Inc.. It received FDA 510(k) clearance on 1982-11-10 under 510(k) number K822984. The device is classified under product code JJT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ID-ZONE LD ISOENZYME CONTROL?

ID-ZONE LD ISOENZYME CONTROL is a medical device that received FDA 510(k) clearance on 1982-11-10. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K822984.

When did ID-ZONE LD ISOENZYME CONTROL receive FDA 510(k) clearance?

ID-ZONE LD ISOENZYME CONTROL received FDA 510(k) clearance on 1982-11-10, under 510(k) number K822984.

Who is the listed applicant for ID-ZONE LD ISOENZYME CONTROL?

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

What is the FDA product code for ID-ZONE LD ISOENZYME CONTROL?

The FDA product code for ID-ZONE LD ISOENZYME CONTROL is JJT.

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Related Devices (Code: JJT)

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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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