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FDA 510(k)

ROUND-BEEHIVE- DISSECTORS 3/8

K-Number: K831912 · 1983-10-31

Decision Date1983-10-31
Product CodeGDI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ROUND-BEEHIVE- DISSECTORS 3/8 is the device name listed in this FDA 510(k) record. The listed applicant is Ormed Mfg., Inc.. It received FDA 510(k) clearance on 1983-10-31 under 510(k) number K831912. The device is classified under product code GDI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 23 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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