ROUND-BEEHIVE- DISSECTORS 3/8
K-Number: K831912 · 1983-10-31
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Device Summary
Frequently Asked Questions
What is the ROUND-BEEHIVE- DISSECTORS 3/8?
ROUND-BEEHIVE- DISSECTORS 3/8 is a medical device that received FDA 510(k) clearance on 1983-10-31. The listed applicant is Ormed Mfg., Inc.. The 510(k) number is K831912.
When did ROUND-BEEHIVE- DISSECTORS 3/8 receive FDA 510(k) clearance?
ROUND-BEEHIVE- DISSECTORS 3/8 received FDA 510(k) clearance on 1983-10-31, under 510(k) number K831912.
Who is the listed applicant for ROUND-BEEHIVE- DISSECTORS 3/8?
The FDA 510(k) record lists Ormed Mfg., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ROUND-BEEHIVE- DISSECTORS 3/8?
The FDA product code for ROUND-BEEHIVE- DISSECTORS 3/8 is GDI.
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 Ormed Mfg., 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: GDI)
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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