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FDA 510(k)

NOMOS MOTORIZED CRANE II

K-Number: K013036 · 2001-12-07

ApplicantNomos Corp.
Decision Date2001-12-07
Product CodeJAI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

NOMOS MOTORIZED CRANE II is the device name listed in this FDA 510(k) record. The listed applicant is Nomos Corp.. It received FDA 510(k) clearance on 2001-12-07 under 510(k) number K013036. 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 NOMOS MOTORIZED CRANE II?

NOMOS MOTORIZED CRANE II is a medical device that received FDA 510(k) clearance on 2001-12-07. The listed applicant is Nomos Corp.. The 510(k) number is K013036.

When did NOMOS MOTORIZED CRANE II receive FDA 510(k) clearance?

NOMOS MOTORIZED CRANE II received FDA 510(k) clearance on 2001-12-07, under 510(k) number K013036.

Who is the listed applicant for NOMOS MOTORIZED CRANE II?

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 NOMOS MOTORIZED CRANE II?

The FDA product code for NOMOS MOTORIZED CRANE II 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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