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FDA 510(k)

REUSABLE LAPAROSCOPIC INSTRUMENTS W/ ELECTROCAUTERY

K-Number: K930666 · 1994-05-19

ApplicantSnowden-Pencer
Decision Date1994-05-19
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

REUSABLE LAPAROSCOPIC INSTRUMENTS W/ ELECTROCAUTERY is the device name listed in this FDA 510(k) record. The listed applicant is Snowden-Pencer. It received FDA 510(k) clearance on 1994-05-19 under 510(k) number K930666. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REUSABLE LAPAROSCOPIC INSTRUMENTS W/ ELECTROCAUTERY?

REUSABLE LAPAROSCOPIC INSTRUMENTS W/ ELECTROCAUTERY is a medical device that received FDA 510(k) clearance on 1994-05-19. The listed applicant is Snowden-Pencer. The 510(k) number is K930666.

When did REUSABLE LAPAROSCOPIC INSTRUMENTS W/ ELECTROCAUTERY receive FDA 510(k) clearance?

REUSABLE LAPAROSCOPIC INSTRUMENTS W/ ELECTROCAUTERY received FDA 510(k) clearance on 1994-05-19, under 510(k) number K930666.

Who is the listed applicant for REUSABLE LAPAROSCOPIC INSTRUMENTS W/ ELECTROCAUTERY?

The FDA 510(k) record lists Snowden-Pencer as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REUSABLE LAPAROSCOPIC INSTRUMENTS W/ ELECTROCAUTERY?

The FDA product code for REUSABLE LAPAROSCOPIC INSTRUMENTS W/ ELECTROCAUTERY is GEI.

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Other records listing Snowden-Pencer 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.

K960400DIAMOND-TOUCH AND MICRO DIAMOND-TOUCH INSTRUMENTS/DIAMOND-LINE INSTRUMENTS/DIAMOND-PORT(ACCESS PARTS)K930667REUSABLE LAPAROSCOPIC INSTRUMENTSK924148DIAMOND-SHARP(R) TROCARSK924149ENDO I/A PROBEK920985SNOWDEN-PENCER IRRIGATION PUMPK920986SNOWDEN-PENCER HIGH FLOW INSUFFLATOR, SP/88-9700

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Related Devices (Code: GEI)

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.

K261959Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, 70mm Blade, Push Button Switch (0703-046-100);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, Push Button Switch, Bulk Non-Sterile (0703-046-102);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, 70mm Blade, Rocker Switch (0703-047-100);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, Rocker Switch, Bulk Non-Sterile (0703-047-102)Stryker InstrumentsK254196HARMONIC 1100 Shears (HAR1120); HARMONIC 1100 Shears (HAR1136)Ethicon Endo-Surgery, LLCK261070LigaSure™ RAS Maryland Jaw Vessel Sealer/Divider, Nano-coatedCovidien, LLCK254185Potenza PrimeJeisys Medical IncorporatedK262364Ellian Enigma RF DeviceEllian CorpK253859Scarlet Pro (Scarlet Pro)VIOL Co., Ltd.

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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