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FDA 510(k)

ARTHROSCOPIC FAT PAD RETRACTOR

K-Number: K802599 · 1980-10-31

ApplicantThe Anspach Effort, Inc.
Decision Date1980-10-31
Product CodeGAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ARTHROSCOPIC FAT PAD RETRACTOR is the device name listed in this FDA 510(k) record. The listed applicant is The Anspach Effort, Inc.. It received FDA 510(k) clearance on 1980-10-31 under 510(k) number K802599. 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 ARTHROSCOPIC FAT PAD RETRACTOR?

ARTHROSCOPIC FAT PAD RETRACTOR is a medical device that received FDA 510(k) clearance on 1980-10-31. The listed applicant is The Anspach Effort, Inc.. The 510(k) number is K802599.

When did ARTHROSCOPIC FAT PAD RETRACTOR receive FDA 510(k) clearance?

ARTHROSCOPIC FAT PAD RETRACTOR received FDA 510(k) clearance on 1980-10-31, under 510(k) number K802599.

Who is the listed applicant for ARTHROSCOPIC FAT PAD RETRACTOR?

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

What is the FDA product code for ARTHROSCOPIC FAT PAD RETRACTOR?

The FDA product code for ARTHROSCOPIC FAT PAD RETRACTOR is GAD.

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Other records listing The Anspach Effort, Inc. as applicant

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K220485Wireless Hand Control, EG1A (WIRELESS-HC), Receiver for Wireless Hand Control, EG1A (RECEIVER-HC)K183545Anspach Helix Dissection ToolsK180063OCM-G1 AttachmentK131053ANSPACH XMAX, EMAX2 AND EMAX2 PLUS SYSTEM WITH OTOLOGIC ATTACHMENT SYSTEMK113476ANSPACH DISSECTION TOOLSK082637CRANIAL PERFORATOR

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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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