Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

AESCULAP SKIN GRAFT MESHER

K-Number: K936186 · 1994-03-10

ApplicantAesculap, Inc.
Decision Date1994-03-10
Product CodeFZW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AESCULAP SKIN GRAFT MESHER is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 1994-03-10 under 510(k) number K936186. The device is classified under product code FZW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AESCULAP SKIN GRAFT MESHER?

AESCULAP SKIN GRAFT MESHER is a medical device that received FDA 510(k) clearance on 1994-03-10. The listed applicant is Aesculap, Inc.. The 510(k) number is K936186.

When did AESCULAP SKIN GRAFT MESHER receive FDA 510(k) clearance?

AESCULAP SKIN GRAFT MESHER received FDA 510(k) clearance on 1994-03-10, under 510(k) number K936186.

Who is the listed applicant for AESCULAP SKIN GRAFT MESHER?

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 SKIN GRAFT MESHER?

The FDA product code for AESCULAP SKIN GRAFT MESHER is FZW.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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

View all 195 devices →

Related Devices (Code: FZW)

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.

K080158LB MEDICAL INFLATABLE TISSUE ELEVATOR/EXPANDER SYSTEMLb Medical LLCK984448BIRCOLL BALLOON DISSECTORWells Johnson Co.K972109SPACEMAKER SURGICALBALLOON DISSECTOR/EXPANDERGeneral Surgical InnovationsK904265INAMED RUIZ-COHEN INTRAOPERATIVE TISSUE EXPANDERInamed Development Co.K902349SURGITEK INTRA-SPAN INTRAOPERATIVE TISSUE EXPANDERSurgitekK883303MENTOR RAPID-SPAN (TM) TISSUE EXPANDERMentor Corp.

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.

↑