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FDA 510(k)

SELF RETAINING RETRACTOR FOR HAND SURG

K-Number: K820290 · 1982-03-05

ApplicantThe Anspach Effort, Inc.
Decision Date1982-03-05
Product CodeGAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SELF RETAINING RETRACTOR FOR HAND SURG 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 1982-03-05 under 510(k) number K820290. 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 SELF RETAINING RETRACTOR FOR HAND SURG?

SELF RETAINING RETRACTOR FOR HAND SURG is a medical device that received FDA 510(k) clearance on 1982-03-05. The listed applicant is The Anspach Effort, Inc.. The 510(k) number is K820290.

When did SELF RETAINING RETRACTOR FOR HAND SURG receive FDA 510(k) clearance?

SELF RETAINING RETRACTOR FOR HAND SURG received FDA 510(k) clearance on 1982-03-05, under 510(k) number K820290.

Who is the listed applicant for SELF RETAINING RETRACTOR FOR HAND SURG?

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 SELF RETAINING RETRACTOR FOR HAND SURG?

The FDA product code for SELF RETAINING RETRACTOR FOR HAND SURG is GAD.

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Other records listing The Anspach Effort, 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.

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)

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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