Decision Date1997-11-06
Product CodeLZA
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
MEDI-PLUS, HEALTH-PLUS, SANITEX, RELIANCE is the device name listed in this FDA 510(k) record. The listed applicant is Pwa Industries Sdn. Bhd.. It received FDA 510(k) clearance on 1997-11-06 under 510(k) number K973551. The device is classified under product code LZA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the MEDI-PLUS, HEALTH-PLUS, SANITEX, RELIANCE?
MEDI-PLUS, HEALTH-PLUS, SANITEX, RELIANCE is a medical device that received FDA 510(k) clearance on 1997-11-06. The listed applicant is Pwa Industries Sdn. Bhd.. The 510(k) number is K973551.
When did MEDI-PLUS, HEALTH-PLUS, SANITEX, RELIANCE receive FDA 510(k) clearance?
MEDI-PLUS, HEALTH-PLUS, SANITEX, RELIANCE received FDA 510(k) clearance on 1997-11-06, under 510(k) number K973551.
Who is the listed applicant for MEDI-PLUS, HEALTH-PLUS, SANITEX, RELIANCE?
The FDA 510(k) record lists Pwa Industries Sdn. Bhd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MEDI-PLUS, HEALTH-PLUS, SANITEX, RELIANCE?
The FDA product code for MEDI-PLUS, HEALTH-PLUS, SANITEX, RELIANCE is LZA.
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Other records listing Pwa Industries Sdn. Bhd. 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.
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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.