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FDA 510(k)

TEKDYNE MICRO RETRACTOR

K-Number: K910975 · 1991-04-01

ApplicantTekdyne
Decision Date1991-04-01
Product CodeGAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TEKDYNE MICRO RETRACTOR is the device name listed in this FDA 510(k) record. The listed applicant is Tekdyne. It received FDA 510(k) clearance on 1991-04-01 under 510(k) number K910975. 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 TEKDYNE MICRO RETRACTOR?

TEKDYNE MICRO RETRACTOR is a medical device that received FDA 510(k) clearance on 1991-04-01. The listed applicant is Tekdyne. The 510(k) number is K910975.

When did TEKDYNE MICRO RETRACTOR receive FDA 510(k) clearance?

TEKDYNE MICRO RETRACTOR received FDA 510(k) clearance on 1991-04-01, under 510(k) number K910975.

Who is the listed applicant for TEKDYNE MICRO RETRACTOR?

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

What is the FDA product code for TEKDYNE MICRO RETRACTOR?

The FDA product code for TEKDYNE MICRO RETRACTOR is GAD.

Related Clinical Trials

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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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