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FDA 510(k)

MURSE RETRACTOR

K-Number: K882112 · 1988-06-15

ApplicantEuro-American Marketing Group, Inc.
Decision Date1988-06-15
Product CodeGAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MURSE RETRACTOR is the device name listed in this FDA 510(k) record. The listed applicant is Euro-American Marketing Group, Inc.. It received FDA 510(k) clearance on 1988-06-15 under 510(k) number K882112. 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 MURSE RETRACTOR?

MURSE RETRACTOR is a medical device that received FDA 510(k) clearance on 1988-06-15. The listed applicant is Euro-American Marketing Group, Inc.. The 510(k) number is K882112.

When did MURSE RETRACTOR receive FDA 510(k) clearance?

MURSE RETRACTOR received FDA 510(k) clearance on 1988-06-15, under 510(k) number K882112.

Who is the listed applicant for MURSE RETRACTOR?

The FDA 510(k) record lists Euro-American Marketing Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MURSE RETRACTOR?

The FDA product code for MURSE RETRACTOR is GAD.

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.

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Other records listing Euro-American Marketing Group, 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.

K903164EURAMARK 610 PHOTOMETERK894856CARDIOPHONE

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

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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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