Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

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 a medical device manufactured by Alpha-Omega Services, Inc.. It received FDA 510(k) clearance on 2024-07-10 under approval 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. It is manufactured by Alpha-Omega Services, Inc.. The 510(k) number is K233628.

When was AOS Interstitial Templates, Needles, and Accessories approved by the FDA?

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

What company makes AOS Interstitial Templates, Needles, and Accessories?

AOS Interstitial Templates, Needles, and Accessories is manufactured by Alpha-Omega Services, Inc..

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 Devices by Alpha-Omega Services, Inc.

K233626AOS Marker Seeds (SMG0242-025)

Related Devices (Code: JAQ)

K160045Heyman Packing Applicator SetVarian Medical Systems, Inc. K161540Advanced Breast Template SystemVarian Medical Systems, Inc. K161576Esophagus Bougie SetVarian Medical Systems, Inc. K160516Universal Cylinder Applicator Family, Universal Segmented Cylinder Applicator Set, Universal Stump Applicator Set, Universal Cervix Probe Set, odd lengths, Universal Cervix Probe Set, even lengthsVarian Medical Systems, Inc. K150979CT/MR Compatible M.A.C. Interstitial GYN TemplateMick Radio-Nuclear Instruments, Inc. K160021Varian Sterilization BoxesVarian Medical Systems, Inc.

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.

↑