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)

Autoclave Indicator Tape; EO Indicator Tape

K-Number: K241036 · 2024-12-17

Decision Date2024-12-17
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Autoclave Indicator Tape; EO Indicator Tape is a medical device manufactured by Jiangmen New Era External Use Drug Co., Ltd.. It received FDA 510(k) clearance on 2024-12-17 under approval number K241036. The device is classified under product code JOJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Autoclave Indicator Tape; EO Indicator Tape?

Autoclave Indicator Tape; EO Indicator Tape is a medical device that received FDA 510(k) clearance on 2024-12-17. It is manufactured by Jiangmen New Era External Use Drug Co., Ltd.. The 510(k) number is K241036.

When was Autoclave Indicator Tape; EO Indicator Tape approved by the FDA?

Autoclave Indicator Tape; EO Indicator Tape received FDA 510(k) clearance on 2024-12-17, under approval number K241036.

What company makes Autoclave Indicator Tape; EO Indicator Tape?

Autoclave Indicator Tape; EO Indicator Tape is manufactured by Jiangmen New Era External Use Drug Co., Ltd..

What is the FDA product code for Autoclave Indicator Tape; EO Indicator Tape?

The FDA product code for Autoclave Indicator Tape; EO Indicator Tape is JOJ.

Related Devices (Code: JOJ)

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.