UPDATED MANUAL FOR PEDS - PULMONARY EVAL. & DIAG.
K-Number: K881122 · 1988-06-10
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Device Summary
Frequently Asked Questions
What is the UPDATED MANUAL FOR PEDS - PULMONARY EVAL. & DIAG.?
UPDATED MANUAL FOR PEDS - PULMONARY EVAL. & DIAG. is a medical device that received FDA 510(k) clearance on 1988-06-10. The listed applicant is Medical Associated Services, Inc.. The 510(k) number is K881122.
When did UPDATED MANUAL FOR PEDS - PULMONARY EVAL. & DIAG. receive FDA 510(k) clearance?
UPDATED MANUAL FOR PEDS - PULMONARY EVAL. & DIAG. received FDA 510(k) clearance on 1988-06-10, under 510(k) number K881122.
Who is the listed applicant for UPDATED MANUAL FOR PEDS - PULMONARY EVAL. & DIAG.?
The FDA 510(k) record lists Medical Associated Services, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UPDATED MANUAL FOR PEDS - PULMONARY EVAL. & DIAG.?
The FDA product code for UPDATED MANUAL FOR PEDS - PULMONARY EVAL. & DIAG. is BTY.
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 Medical Associated Services, Inc. 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: BTY)
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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