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FDA 510(k)

DIGITOXIN

K-Number: K780495 · 1978-04-10

ApplicantDiagnostic Products Corp.
Decision Date1978-04-10
Product CodeDJK
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

DIGITOXIN is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Products Corp.. It received FDA 510(k) clearance on 1978-04-10 under 510(k) number K780495. The device is classified under product code DJK. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGITOXIN?

DIGITOXIN is a medical device that received FDA 510(k) clearance on 1978-04-10. The listed applicant is Diagnostic Products Corp.. The 510(k) number is K780495.

When did DIGITOXIN receive FDA 510(k) clearance?

DIGITOXIN received FDA 510(k) clearance on 1978-04-10, under 510(k) number K780495.

Who is the listed applicant for DIGITOXIN?

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

What is the FDA product code for DIGITOXIN?

The FDA product code for DIGITOXIN is DJK.

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Other records listing Diagnostic Products Corp. 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.

K063045IMMULITE 2000, IMMULITE 2500 VANCOMYCINK034055IMMULITE 2500 CK-MB, 2500 MYOGLOBIN, 2500 STAT TROPONIN IK033234IMMULITE 2500 AUTOMATED IMMUNOASSAY ANALYZERK032881IMMULITE/IMMULITE 1000 TOTAL TESTOSTERONE AND IMMULITE 2000 TOTAL TESTOSTERONEK023152IMMULITE 2000 ALLERGEN-SPECIFIC IGEK023304IMMULITE/IMMULITE 1000 CALCITONIN, MODEL LKCL AND IMMULITE 2000 CALCITONIN, MODEL L2KCL

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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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