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FDA 510(k)

AOS Interstitial Templates, Needles, and Accessories

K-Number: K233628 · 2024-07-10

ApplicantAlpha-Omega Services, Inc.
Decision Date2024-07-10
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AOS Interstitial Templates, Needles, and Accessories is the device name listed in this FDA 510(k) record. The listed applicant is Alpha-Omega Services, Inc.. It received FDA 510(k) clearance on 2024-07-10 under 510(k) number K233628. The device is classified under product code JAQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AOS Interstitial Templates, Needles, and Accessories?

AOS Interstitial Templates, Needles, and Accessories is a medical device that received FDA 510(k) clearance on 2024-07-10. The listed applicant is Alpha-Omega Services, Inc.. The 510(k) number is K233628.

When did AOS Interstitial Templates, Needles, and Accessories receive FDA 510(k) clearance?

AOS Interstitial Templates, Needles, and Accessories received FDA 510(k) clearance on 2024-07-10, under 510(k) number K233628.

Who is the listed applicant for AOS Interstitial Templates, Needles, and Accessories?

The FDA 510(k) record lists Alpha-Omega Services, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AOS Interstitial Templates, Needles, and Accessories?

The FDA product code for AOS Interstitial Templates, Needles, and Accessories is JAQ.

Other records listing Alpha-Omega Services, Inc. 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.

K233626AOS Marker Seeds (SMG0242-025)

Related Devices (Code: JAQ)

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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