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FDA 510(k)

MODIFIED ROUND (BEEHIVE) DISSECTOR 3/8

K-Number: K873391 · 1987-09-11

ApplicantOrmed Mfg., Inc.
Decision Date1987-09-11
Product CodeGDY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MODIFIED ROUND (BEEHIVE) DISSECTOR 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 1987-09-11 under 510(k) number K873391. The device is classified under product code GDY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED ROUND (BEEHIVE) DISSECTOR 3/8?

MODIFIED ROUND (BEEHIVE) DISSECTOR 3/8 is a medical device that received FDA 510(k) clearance on 1987-09-11. The listed applicant is Ormed Mfg., Inc.. The 510(k) number is K873391.

When did MODIFIED ROUND (BEEHIVE) DISSECTOR 3/8 receive FDA 510(k) clearance?

MODIFIED ROUND (BEEHIVE) DISSECTOR 3/8 received FDA 510(k) clearance on 1987-09-11, under 510(k) number K873391.

Who is the listed applicant for MODIFIED ROUND (BEEHIVE) DISSECTOR 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 MODIFIED ROUND (BEEHIVE) DISSECTOR 3/8?

The FDA product code for MODIFIED ROUND (BEEHIVE) DISSECTOR 3/8 is GDY.

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Other records listing Ormed Mfg., Inc. as applicant

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Related Devices (Code: GDY)

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.

K972634ULTRACELL SUCTION SPONGEUltracell Medical Technologies, Inc.K960236CPR LAP SPONGESCustom Pack ReliabilityK955599STRYKER FEMORAL CANAL SPONGE & ACETABULUM SPONGEStryker Corp.K955322PROTEC X-RAY DETECTABLE GAUZE SPONGEDerivados DE Gasa, S.A. DE C.V.K953830KENSORBKentron Health Care, Inc.K953059KITTNER DISSECTORMedical Perspectives Corp.

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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