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FDA 510(k)

KANDI-NUCLEAR MED. DATA ACQU.&INFO.

K-Number: K800835 · 1980-05-28

ApplicantKrupp International, Inc.
Decision Date1980-05-28
Product Code
DecisionSubstantially Equivalent

Device Summary

KANDI-NUCLEAR MED. DATA ACQU.&INFO. is the device name listed in this FDA 510(k) record. The listed applicant is Krupp International, Inc.. It received FDA 510(k) clearance on 1980-05-28 under 510(k) number K800835. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KANDI-NUCLEAR MED. DATA ACQU.&INFO.?

KANDI-NUCLEAR MED. DATA ACQU.&INFO. is a medical device that received FDA 510(k) clearance on 1980-05-28. The listed applicant is Krupp International, Inc.. The 510(k) number is K800835.

When did KANDI-NUCLEAR MED. DATA ACQU.&INFO. receive FDA 510(k) clearance?

KANDI-NUCLEAR MED. DATA ACQU.&INFO. received FDA 510(k) clearance on 1980-05-28, under 510(k) number K800835.

Who is the listed applicant for KANDI-NUCLEAR MED. DATA ACQU.&INFO.?

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

Related Clinical Trials

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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Other records listing Krupp International, Inc. 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.

K780090DENTAL ALLOY

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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