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FDA 510(k)

AESCULAP SURGICAL ACCESSORIES

K-Number: K913262 · 1991-12-30

ApplicantAesculap, Inc.
Decision Date1991-12-30
Product CodeGEY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AESCULAP SURGICAL ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 1991-12-30 under 510(k) number K913262. The device is classified under product code GEY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AESCULAP SURGICAL ACCESSORIES?

AESCULAP SURGICAL ACCESSORIES is a medical device that received FDA 510(k) clearance on 1991-12-30. The listed applicant is Aesculap, Inc.. The 510(k) number is K913262.

When did AESCULAP SURGICAL ACCESSORIES receive FDA 510(k) clearance?

AESCULAP SURGICAL ACCESSORIES received FDA 510(k) clearance on 1991-12-30, under 510(k) number K913262.

Who is the listed applicant for AESCULAP SURGICAL ACCESSORIES?

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

What is the FDA product code for AESCULAP SURGICAL ACCESSORIES?

The FDA product code for AESCULAP SURGICAL ACCESSORIES is GEY.

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Other records listing Aesculap, 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.

K242762Aesculap Aicon® Series Container SystemK242003XABO Ventricular Catheter, XABO Peritoneal Catheter, XABO Catheter SetK223596SQ.line KERRISONK214041Aesculap AICON ContainerK211572Aesculap Slim Clip ApplierK203739ELAN 4 Electro Motor System

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Related Devices (Code: GEY)

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.

K050519ADVANCED TURBO DRIVE SYSTEMLinvatec Corp.K020621ARTHROCARE CONTROLLER; ARTHROCARE CABLE; FOOT CONTROL; POWER CORD; WANDSArthrocare Corp.K012738SYMPHONY GRAFT DELIVERY SYSTEM (GDS)DepuyacromedK972308MEDNEXT 1000 DRILLMednext, Inc.K971941AQUA SPRAYBoyd Industries, Inc.K971782BONE AND MARROW COLLECTION SYSTEM KITBiomedical Ent., Inc.

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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