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FDA 510(k)

IDI GDR DATA REDUCTION SYSTEM

K-Number: K780813 · 1978-06-28

ApplicantIso-Data, Inc.
Decision Date1978-06-28
Product Code
DecisionSubstantially Equivalent

Device Summary

IDI GDR DATA REDUCTION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Iso-Data, Inc.. It received FDA 510(k) clearance on 1978-06-28 under 510(k) number K780813. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IDI GDR DATA REDUCTION SYSTEM?

IDI GDR DATA REDUCTION SYSTEM is a medical device that received FDA 510(k) clearance on 1978-06-28. The listed applicant is Iso-Data, Inc.. The 510(k) number is K780813.

When did IDI GDR DATA REDUCTION SYSTEM receive FDA 510(k) clearance?

IDI GDR DATA REDUCTION SYSTEM received FDA 510(k) clearance on 1978-06-28, under 510(k) number K780813.

Who is the listed applicant for IDI GDR DATA REDUCTION SYSTEM?

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

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Other records listing Iso-Data, 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.

K872429ISO-DATA 100 SERIES GAMMA COUNTERK872430ISO-DATA 500 SERIES GAMMA COUNTERK843434ISO-DATA CENTRIFUGES 1-A, 101, 2D, ETC.K843365ISO-DATA IMMUNOASSAY NETWORK SYSTEMK810631DPM CALCULATORK780790IDI 200 GAMMA COUNTER

View all 7 devices →

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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