OPPORTUNITY INC. BONE MARROW BIOPSY AND ASPIRATION TRAY
K-Number: K971061 · 1997-06-11
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Device Summary
Frequently Asked Questions
What is the OPPORTUNITY INC. BONE MARROW BIOPSY AND ASPIRATION TRAY?
OPPORTUNITY INC. BONE MARROW BIOPSY AND ASPIRATION TRAY is a medical device that received FDA 510(k) clearance on 1997-06-11. The listed applicant is Opportunity, Inc.. The 510(k) number is K971061.
When did OPPORTUNITY INC. BONE MARROW BIOPSY AND ASPIRATION TRAY receive FDA 510(k) clearance?
OPPORTUNITY INC. BONE MARROW BIOPSY AND ASPIRATION TRAY received FDA 510(k) clearance on 1997-06-11, under 510(k) number K971061.
Who is the listed applicant for OPPORTUNITY INC. BONE MARROW BIOPSY AND ASPIRATION TRAY?
The FDA 510(k) record lists Opportunity, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OPPORTUNITY INC. BONE MARROW BIOPSY AND ASPIRATION TRAY?
The FDA product code for OPPORTUNITY INC. BONE MARROW BIOPSY AND ASPIRATION TRAY is LRO.
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 Opportunity, 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: LRO)
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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