Altomed Malhotra Platinum Segments
K-Number: K170591 · 2017-06-06
ApplicantAltomed Limited
Decision Date2017-06-06
Product CodeMML
Advisory CommitteeOP
DecisionSubstantially Equivalent
Device Summary
Altomed Malhotra Platinum Segments is a medical device manufactured by Altomed Limited. It received FDA 510(k) clearance on 2017-06-06 under approval number K170591. The device is classified under product code MML. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Altomed Malhotra Platinum Segments?
Altomed Malhotra Platinum Segments is a medical device that received FDA 510(k) clearance on 2017-06-06. It is manufactured by Altomed Limited. The 510(k) number is K170591.
When was Altomed Malhotra Platinum Segments approved by the FDA?
Altomed Malhotra Platinum Segments received FDA 510(k) clearance on 2017-06-06, under approval number K170591.
What company makes Altomed Malhotra Platinum Segments?
Altomed Malhotra Platinum Segments is manufactured by Altomed Limited.
What is the FDA product code for Altomed Malhotra Platinum Segments?
The FDA product code for Altomed Malhotra Platinum Segments is MML.
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.