PNEUMATIC DEMAND OXYGEN CONSERVER (PDOC)
K-Number: K990678 · 1999-05-07
Advertisement
Device Summary
Frequently Asked Questions
What is the PNEUMATIC DEMAND OXYGEN CONSERVER (PDOC)?
PNEUMATIC DEMAND OXYGEN CONSERVER (PDOC) is a medical device that received FDA 510(k) clearance on 1999-05-07. The listed applicant is Salter Labs. The 510(k) number is K990678.
When did PNEUMATIC DEMAND OXYGEN CONSERVER (PDOC) receive FDA 510(k) clearance?
PNEUMATIC DEMAND OXYGEN CONSERVER (PDOC) received FDA 510(k) clearance on 1999-05-07, under 510(k) number K990678.
Who is the listed applicant for PNEUMATIC DEMAND OXYGEN CONSERVER (PDOC)?
The FDA 510(k) record lists Salter Labs as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PNEUMATIC DEMAND OXYGEN CONSERVER (PDOC)?
The FDA product code for PNEUMATIC DEMAND OXYGEN CONSERVER (PDOC) is NFB.
Related Clinical Trials
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.
Other records listing Salter Labs 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.
Related Devices (Code: NFB)
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.
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.
Advertisement