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FDA 510(k)

OMNI-TRACT SURGICAL RETRACTOR SYS

K-Number: K842762 · 1984-08-17

ApplicantMinnesota Scientific, Inc.
Decision Date1984-08-17
Product CodeGAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

OMNI-TRACT SURGICAL RETRACTOR SYS is the device name listed in this FDA 510(k) record. The listed applicant is Minnesota Scientific, Inc.. It received FDA 510(k) clearance on 1984-08-17 under 510(k) number K842762. The device is classified under product code GAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OMNI-TRACT SURGICAL RETRACTOR SYS?

OMNI-TRACT SURGICAL RETRACTOR SYS is a medical device that received FDA 510(k) clearance on 1984-08-17. The listed applicant is Minnesota Scientific, Inc.. The 510(k) number is K842762.

When did OMNI-TRACT SURGICAL RETRACTOR SYS receive FDA 510(k) clearance?

OMNI-TRACT SURGICAL RETRACTOR SYS received FDA 510(k) clearance on 1984-08-17, under 510(k) number K842762.

Who is the listed applicant for OMNI-TRACT SURGICAL RETRACTOR SYS?

The FDA 510(k) record lists Minnesota Scientific, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OMNI-TRACT SURGICAL RETRACTOR SYS?

The FDA product code for OMNI-TRACT SURGICAL RETRACTOR SYS is GAD.

Related Clinical Trials

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Other records listing Minnesota Scientific, 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.

K872919OMNI-TRACT CORRAL RETRACTORK853948MINNESOTA SCIENTIFIC, INC. OMNI-BEAMK853947OMNI-TRACT CHEST WALL & LUNA RETRACTORK810282OPERATING TABLE ACCESSORY CLAMP

Related Devices (Code: GAD)

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.

K152538JRP Wound SpreaderJ.R. Parker, LLCK151104OTELO LLSpineartK132645THORATRAK MICS RETRACTOR SYSTEM, RACK, BLADESMedtronic, Inc.K071775DASHEzsurgicalK050256APPLE MEDICAL/OB MOBIUS ELASTIC RETRACTORApple Medical Corp.K043602QUADRANT RETRACTOR SYSTEMMedtronic Sofamor Danek

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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