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FDA 510(k)

THE NOMOS MINICRANE

K-Number: K964740 · 1997-02-11

ApplicantNomos Corp.
Decision Date1997-02-11
Product CodeJAI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

THE NOMOS MINICRANE is the device name listed in this FDA 510(k) record. The listed applicant is Nomos Corp.. It received FDA 510(k) clearance on 1997-02-11 under 510(k) number K964740. The device is classified under product code JAI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE NOMOS MINICRANE?

THE NOMOS MINICRANE is a medical device that received FDA 510(k) clearance on 1997-02-11. The listed applicant is Nomos Corp.. The 510(k) number is K964740.

When did THE NOMOS MINICRANE receive FDA 510(k) clearance?

THE NOMOS MINICRANE received FDA 510(k) clearance on 1997-02-11, under 510(k) number K964740.

Who is the listed applicant for THE NOMOS MINICRANE?

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

What is the FDA product code for THE NOMOS MINICRANE?

The FDA product code for THE NOMOS MINICRANE is JAI.

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Other records listing Nomos 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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