SPIROMETER MODEL TS-200 SLZ 7541
K-Number: K855070 · 1986-01-30
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Device Summary
Frequently Asked Questions
What is the SPIROMETER MODEL TS-200 SLZ 7541?
SPIROMETER MODEL TS-200 SLZ 7541 is a medical device that received FDA 510(k) clearance on 1986-01-30. The listed applicant is Teledyne Avionics Div. of Teledyne. The 510(k) number is K855070.
When did SPIROMETER MODEL TS-200 SLZ 7541 receive FDA 510(k) clearance?
SPIROMETER MODEL TS-200 SLZ 7541 received FDA 510(k) clearance on 1986-01-30, under 510(k) number K855070.
Who is the listed applicant for SPIROMETER MODEL TS-200 SLZ 7541?
The FDA 510(k) record lists Teledyne Avionics Div. of Teledyne as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SPIROMETER MODEL TS-200 SLZ 7541?
The FDA product code for SPIROMETER MODEL TS-200 SLZ 7541 is BZC.
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 Teledyne Avionics Div. of Teledyne 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: BZC)
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.
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