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FDA 510(k)

DISPOSABLE #11 SCALPEL BLADE W/SHORT

K-Number: K820869 · 1982-05-05

ApplicantVan-Tec, Inc.
Decision Date1982-05-05
Product CodeGDX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE #11 SCALPEL BLADE W/SHORT is the device name listed in this FDA 510(k) record. The listed applicant is Van-Tec, Inc.. It received FDA 510(k) clearance on 1982-05-05 under 510(k) number K820869. The device is classified under product code GDX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE #11 SCALPEL BLADE W/SHORT?

DISPOSABLE #11 SCALPEL BLADE W/SHORT is a medical device that received FDA 510(k) clearance on 1982-05-05. The listed applicant is Van-Tec, Inc.. The 510(k) number is K820869.

When did DISPOSABLE #11 SCALPEL BLADE W/SHORT receive FDA 510(k) clearance?

DISPOSABLE #11 SCALPEL BLADE W/SHORT received FDA 510(k) clearance on 1982-05-05, under 510(k) number K820869.

Who is the listed applicant for DISPOSABLE #11 SCALPEL BLADE W/SHORT?

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

What is the FDA product code for DISPOSABLE #11 SCALPEL BLADE W/SHORT?

The FDA product code for DISPOSABLE #11 SCALPEL BLADE W/SHORT is GDX.

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Other records listing Van-Tec, 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.

K880099VAN-TEC BLADDER EVACUATORK880095BERGER PROSTATE CULTURE CYTOLOGY BRUSHK880096VAN-TEC ASPIRATION BIOPSY SYSTEM W/COLLECTION CUPK880098VAN-TEC AUTO BIOPSY NEEDLEK880094VAN-TEC ENDOPYELOTOMY KNIFEK874112VAN-TEC DOUBLE OCCLUSION BALLOON CATHETER

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Related Devices (Code: GDX)

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.

K923689SURGISTAR BLADESSurgistar, Inc.K921167ULTRABLADEMicron Technology, Inc.K914086ICAN CYLINDRICAL SPONGESIcn Pharmaceuticals, Inc.K904505CCI CORNEAL SCARIFIERBuckman Co., Inc.K9053801-CUT ACL GRAFT KNIFEDepuy, Inc.K895682VESSEL LOOPSApplied Medical Technologies

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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