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FDA 510(k)

SHIMADZU DIGITAL SUBTRACTION SYSTEM DAR-1200

K-Number: K884598 · 1989-04-20

ApplicantShimadzu Precision Instruments, Inc.
Decision Date1989-04-20
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SHIMADZU DIGITAL SUBTRACTION SYSTEM DAR-1200 is the device name listed in this FDA 510(k) record. The listed applicant is Shimadzu Precision Instruments, Inc.. It received FDA 510(k) clearance on 1989-04-20 under 510(k) number K884598. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHIMADZU DIGITAL SUBTRACTION SYSTEM DAR-1200?

SHIMADZU DIGITAL SUBTRACTION SYSTEM DAR-1200 is a medical device that received FDA 510(k) clearance on 1989-04-20. The listed applicant is Shimadzu Precision Instruments, Inc.. The 510(k) number is K884598.

When did SHIMADZU DIGITAL SUBTRACTION SYSTEM DAR-1200 receive FDA 510(k) clearance?

SHIMADZU DIGITAL SUBTRACTION SYSTEM DAR-1200 received FDA 510(k) clearance on 1989-04-20, under 510(k) number K884598.

Who is the listed applicant for SHIMADZU DIGITAL SUBTRACTION SYSTEM DAR-1200?

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

What is the FDA product code for SHIMADZU DIGITAL SUBTRACTION SYSTEM DAR-1200?

The FDA product code for SHIMADZU DIGITAL SUBTRACTION SYSTEM DAR-1200 is JAA.

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Other records listing Shimadzu Precision Instruments, Inc. as applicant

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Related Devices (Code: JAA)

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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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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