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FDA 510(k)

GRASSHOPPER - RETRACTOR

K-Number: K842992 · 1984-08-17

ApplicantNorton Texas Medical Products
Decision Date1984-08-17
Product CodeGAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

GRASSHOPPER - RETRACTOR is the device name listed in this FDA 510(k) record. The listed applicant is Norton Texas Medical Products. It received FDA 510(k) clearance on 1984-08-17 under 510(k) number K842992. 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 GRASSHOPPER - RETRACTOR?

GRASSHOPPER - RETRACTOR is a medical device that received FDA 510(k) clearance on 1984-08-17. The listed applicant is Norton Texas Medical Products. The 510(k) number is K842992.

When did GRASSHOPPER - RETRACTOR receive FDA 510(k) clearance?

GRASSHOPPER - RETRACTOR received FDA 510(k) clearance on 1984-08-17, under 510(k) number K842992.

Who is the listed applicant for GRASSHOPPER - RETRACTOR?

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

What is the FDA product code for GRASSHOPPER - RETRACTOR?

The FDA product code for GRASSHOPPER - 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 Norton Texas Medical Products 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.

K843983MYOCARDIAL INSULATORK842194PRESSURE MONITORK832517CUSTOM KWIK SET AND/OR PAK

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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