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FDA 510(k)

ANATOM 1000 (A MINUS, A-)

K-Number: K974455 · 1998-02-20

ApplicantAnalogic Corp.
Decision Date1998-02-20
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ANATOM 1000 (A MINUS, A-) is the device name listed in this FDA 510(k) record. The listed applicant is Analogic Corp.. It received FDA 510(k) clearance on 1998-02-20 under 510(k) number K974455. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANATOM 1000 (A MINUS, A-)?

ANATOM 1000 (A MINUS, A-) is a medical device that received FDA 510(k) clearance on 1998-02-20. The listed applicant is Analogic Corp.. The 510(k) number is K974455.

When did ANATOM 1000 (A MINUS, A-) receive FDA 510(k) clearance?

ANATOM 1000 (A MINUS, A-) received FDA 510(k) clearance on 1998-02-20, under 510(k) number K974455.

Who is the listed applicant for ANATOM 1000 (A MINUS, A-)?

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

What is the FDA product code for ANATOM 1000 (A MINUS, A-)?

The FDA product code for ANATOM 1000 (A MINUS, A-) is JAK.

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Other records listing Analogic 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.

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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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