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FDA 510(k)

VALLEYLAB FORCE GSU HANDSET ADAPTER MODEL #E0500

K-Number: K933181 · 1993-11-02

ApplicantValleylab, Inc.
Decision Date1993-11-02
Product CodeGFI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VALLEYLAB FORCE GSU HANDSET ADAPTER MODEL #E0500 is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1993-11-02 under 510(k) number K933181. The device is classified under product code GFI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VALLEYLAB FORCE GSU HANDSET ADAPTER MODEL #E0500?

VALLEYLAB FORCE GSU HANDSET ADAPTER MODEL #E0500 is a medical device that received FDA 510(k) clearance on 1993-11-02. The listed applicant is Valleylab, Inc.. The 510(k) number is K933181.

When did VALLEYLAB FORCE GSU HANDSET ADAPTER MODEL #E0500 receive FDA 510(k) clearance?

VALLEYLAB FORCE GSU HANDSET ADAPTER MODEL #E0500 received FDA 510(k) clearance on 1993-11-02, under 510(k) number K933181.

Who is the listed applicant for VALLEYLAB FORCE GSU HANDSET ADAPTER MODEL #E0500?

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

What is the FDA product code for VALLEYLAB FORCE GSU HANDSET ADAPTER MODEL #E0500?

The FDA product code for VALLEYLAB FORCE GSU HANDSET ADAPTER MODEL #E0500 is GFI.

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Other records listing Valleylab, 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.

K031011LIGASURE 5MM LAPAROSCOPIC SEALER-DIVIDER, MODEL LS1500K010010VALLEYLAB LIGASURE PRECISE INSTRUMENT VESSEL SEALING SYSTEM-MODEL # LS1200 & SLIGAURE GENERATORK010013LIGASURE LAPAROSCOPIC SEALER DIVIDER MODEL LS1100K994428E7512 PREMIE REM POLYHESIVE II PATIENT RETURN ELECTRODEK983743BISURE LAPAROSCOPIC BIPOLAR FORCEPSK981916LIGASURE VESSEL SEALING SYSTEM

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Related Devices (Code: GFI)

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.

K932534ISI FENESTRATED DISSECTING AND GRASPING FORCEPSInnovative Surgical, Inc.K920001HEMOLAB SILIMAT REAGENTBiomerieux Vitek, Inc.K891887OSTEOTOMES, VARIOUS TYPESZinnanti Surgical Instruments, Inc.K852541STORZ ION BOND OSTEOTOMES & RASPS, FAST CU BURSStorz Instrument Co.K842823CHERMEL OSTEOTOMESCher Mel 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.

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