QUANTUM 3080SP SURGICAL TABLE
K-Number: K971390 · 1997-05-15
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Device Summary
Frequently Asked Questions
What is the QUANTUM 3080SP SURGICAL TABLE?
QUANTUM 3080SP SURGICAL TABLE is a medical device that received FDA 510(k) clearance on 1997-05-15. The listed applicant is STERIS Corporation. The 510(k) number is K971390.
When did QUANTUM 3080SP SURGICAL TABLE receive FDA 510(k) clearance?
QUANTUM 3080SP SURGICAL TABLE received FDA 510(k) clearance on 1997-05-15, under 510(k) number K971390.
Who is the listed applicant for QUANTUM 3080SP SURGICAL TABLE?
The FDA 510(k) record lists STERIS Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for QUANTUM 3080SP SURGICAL TABLE?
The FDA product code for QUANTUM 3080SP SURGICAL TABLE is GDC.
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 STERIS Corporation 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: GDC)
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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