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FDA 510(k)

RETRACTOR, SKIN HOOK

K-Number: K770418 · 1977-03-23

ApplicantAcme United Corp.
Decision Date1977-03-23
Product CodeGAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RETRACTOR, SKIN HOOK is the device name listed in this FDA 510(k) record. The listed applicant is Acme United Corp.. It received FDA 510(k) clearance on 1977-03-23 under 510(k) number K770418. 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 RETRACTOR, SKIN HOOK?

RETRACTOR, SKIN HOOK is a medical device that received FDA 510(k) clearance on 1977-03-23. The listed applicant is Acme United Corp.. The 510(k) number is K770418.

When did RETRACTOR, SKIN HOOK receive FDA 510(k) clearance?

RETRACTOR, SKIN HOOK received FDA 510(k) clearance on 1977-03-23, under 510(k) number K770418.

Who is the listed applicant for RETRACTOR, SKIN HOOK?

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

What is the FDA product code for RETRACTOR, SKIN HOOK?

The FDA product code for RETRACTOR, SKIN HOOK is GAD.

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Other records listing Acme United Corp. as applicant

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Related Devices (Code: GAD)

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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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