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FDA 510(k)

N/A

K-Number: K970590 · 1997-06-13

Decision Date1997-06-13
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

N/A is the device name listed in this FDA 510(k) record. The listed applicant is North American Technical Services Corp.. It received FDA 510(k) clearance on 1997-06-13 under 510(k) number K970590. The device is classified under product code ILY. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the N/A?

N/A is a medical device that received FDA 510(k) clearance on 1997-06-13. The listed applicant is North American Technical Services Corp.. The 510(k) number is K970590.

When did N/A receive FDA 510(k) clearance?

N/A received FDA 510(k) clearance on 1997-06-13, under 510(k) number K970590.

Who is the listed applicant for N/A?

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

What is the FDA product code for N/A?

The FDA product code for N/A is ILY.

Other records listing North American Technical Services 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 9 devices →

Related Devices (Code: ILY)

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

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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