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FDA 510(k)

KAPPA & LAMBDA BENCE JONES CONTROLS

K-Number: K812327 · 1981-09-01

ApplicantKallestad Laboratories, Inc.
Decision Date1981-09-01
Product CodeCZQ
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

KAPPA & LAMBDA BENCE JONES CONTROLS is the device name listed in this FDA 510(k) record. The listed applicant is Kallestad Laboratories, Inc.. It received FDA 510(k) clearance on 1981-09-01 under 510(k) number K812327. The device is classified under product code CZQ. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KAPPA & LAMBDA BENCE JONES CONTROLS?

KAPPA & LAMBDA BENCE JONES CONTROLS is a medical device that received FDA 510(k) clearance on 1981-09-01. The listed applicant is Kallestad Laboratories, Inc.. The 510(k) number is K812327.

When did KAPPA & LAMBDA BENCE JONES CONTROLS receive FDA 510(k) clearance?

KAPPA & LAMBDA BENCE JONES CONTROLS received FDA 510(k) clearance on 1981-09-01, under 510(k) number K812327.

Who is the listed applicant for KAPPA & LAMBDA BENCE JONES CONTROLS?

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

What is the FDA product code for KAPPA & LAMBDA BENCE JONES CONTROLS?

The FDA product code for KAPPA & LAMBDA BENCE JONES CONTROLS is CZQ.

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Other records listing Kallestad Laboratories, Inc. as applicant

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Related Devices (Code: CZQ)

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.

K802284ANTISERA TO HUMAN FREE LAMBDA LIGHT CH.Kallestad Laboratories, Inc.

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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