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FDA 510(k)

AUTOMATIC RETRACTOR HOLDERS

K-Number: K792145 · 1979-12-05

ApplicantAutomated Medical Products, Inc.
Decision Date1979-12-05
Product CodeGAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AUTOMATIC RETRACTOR HOLDERS is the device name listed in this FDA 510(k) record. The listed applicant is Automated Medical Products, Inc.. It received FDA 510(k) clearance on 1979-12-05 under 510(k) number K792145. 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 HOLDERS?

AUTOMATIC RETRACTOR HOLDERS is a medical device that received FDA 510(k) clearance on 1979-12-05. The listed applicant is Automated Medical Products, Inc.. The 510(k) number is K792145.

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

AUTOMATIC RETRACTOR HOLDERS received FDA 510(k) clearance on 1979-12-05, under 510(k) number K792145.

Who is the listed applicant for AUTOMATIC RETRACTOR HOLDERS?

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

What is the FDA product code for AUTOMATIC RETRACTOR HOLDERS?

The FDA product code for AUTOMATIC RETRACTOR HOLDERS 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 Automated Medical Products, 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.

K832827CORPULS 300

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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