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FDA 510(k)

ETHICON RETRACTION TAPE

K-Number: K801699 · 1980-09-26

ApplicantETHICON, Inc.
Decision Date1980-09-26
Product CodeGAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ETHICON RETRACTION TAPE is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 1980-09-26 under 510(k) number K801699. 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 ETHICON RETRACTION TAPE?

ETHICON RETRACTION TAPE is a medical device that received FDA 510(k) clearance on 1980-09-26. The listed applicant is ETHICON, Inc.. The 510(k) number is K801699.

When did ETHICON RETRACTION TAPE receive FDA 510(k) clearance?

ETHICON RETRACTION TAPE received FDA 510(k) clearance on 1980-09-26, under 510(k) number K801699.

Who is the listed applicant for ETHICON RETRACTION TAPE?

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

What is the FDA product code for ETHICON RETRACTION TAPE?

The FDA product code for ETHICON RETRACTION TAPE is GAD.

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Other records listing ETHICON, Inc. as applicant

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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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