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FDA 510(k)

AUTOMATIC RETRACTOR HOLDER

K-Number: K780708 · 1978-07-17

ApplicantGreat Eastern Lumber Co., Inc.
Decision Date1978-07-17
Product CodeGAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AUTOMATIC RETRACTOR HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Great Eastern Lumber Co., Inc.. It received FDA 510(k) clearance on 1978-07-17 under 510(k) number K780708. 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 AUTOMATIC RETRACTOR HOLDER?

AUTOMATIC RETRACTOR HOLDER is a medical device that received FDA 510(k) clearance on 1978-07-17. The listed applicant is Great Eastern Lumber Co., Inc.. The 510(k) number is K780708.

When did AUTOMATIC RETRACTOR HOLDER receive FDA 510(k) clearance?

AUTOMATIC RETRACTOR HOLDER received FDA 510(k) clearance on 1978-07-17, under 510(k) number K780708.

Who is the listed applicant for AUTOMATIC RETRACTOR HOLDER?

The FDA 510(k) record lists Great Eastern Lumber Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AUTOMATIC RETRACTOR HOLDER?

The FDA product code for AUTOMATIC RETRACTOR HOLDER 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 Great Eastern Lumber Co., 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.

K780999X-RAY FRAME HOLDER

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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