FDA 510(k)

HOOK

K-Number: K841625 · 1984-08-27

Decision Date1984-08-27

Product CodeGAD

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

HOOK is the device name listed in this FDA 510(k) record. The listed applicant is Plastafil, Inc.. It received FDA 510(k) clearance on 1984-08-27 under 510(k) number K841625. 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 HOOK?

HOOK is a medical device that received FDA 510(k) clearance on 1984-08-27. The listed applicant is Plastafil, Inc.. The 510(k) number is K841625.

When did HOOK receive FDA 510(k) clearance?

HOOK received FDA 510(k) clearance on 1984-08-27, under 510(k) number K841625.

Who is the listed applicant for HOOK?

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

What is the FDA product code for HOOK?

The FDA product code for HOOK is GAD.

Other records listing Plastafil, 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.

K841621BACK RADIUS CUTTER K841620FRONT RADIUS CUTTER K841617STROVER HOOK K841626PUNCH K841629DRILL BIT K841627MALLET

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Related Devices (Code: GAD)

K152538JRP Wound SpreaderJ.R. Parker, LLC K151104OTELO LLSpineart K132645THORATRAK MICS RETRACTOR SYSTEM, RACK, BLADESMedtronic, Inc.K071775DASHEzsurgical K050256APPLE 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.