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FDA 510(k)

HITACHI 705 CALIBRATOR

K-Number: K811921 · 1981-07-23

Decision Date1981-07-23
Product CodeJIX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

HITACHI 705 CALIBRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Boehringer Mannheim Corp.. It received FDA 510(k) clearance on 1981-07-23 under 510(k) number K811921. The device is classified under product code JIX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HITACHI 705 CALIBRATOR?

HITACHI 705 CALIBRATOR is a medical device that received FDA 510(k) clearance on 1981-07-23. The listed applicant is Boehringer Mannheim Corp.. The 510(k) number is K811921.

When did HITACHI 705 CALIBRATOR receive FDA 510(k) clearance?

HITACHI 705 CALIBRATOR received FDA 510(k) clearance on 1981-07-23, under 510(k) number K811921.

Who is the listed applicant for HITACHI 705 CALIBRATOR?

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

What is the FDA product code for HITACHI 705 CALIBRATOR?

The FDA product code for HITACHI 705 CALIBRATOR is JIX.

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.

Other records listing Boehringer Mannheim 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.

View all 340 devices →

Related Devices (Code: JIX)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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