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FDA 510(k)

REUSABLE LAPAROSCOPIC INSTRUMENTS

K-Number: K930667 · 1994-05-16

ApplicantSnowden-Pencer
Decision Date1994-05-16
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

REUSABLE LAPAROSCOPIC INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Snowden-Pencer. It received FDA 510(k) clearance on 1994-05-16 under 510(k) number K930667. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REUSABLE LAPAROSCOPIC INSTRUMENTS?

REUSABLE LAPAROSCOPIC INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1994-05-16. The listed applicant is Snowden-Pencer. The 510(k) number is K930667.

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

REUSABLE LAPAROSCOPIC INSTRUMENTS received FDA 510(k) clearance on 1994-05-16, under 510(k) number K930667.

Who is the listed applicant for REUSABLE LAPAROSCOPIC INSTRUMENTS?

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?

The FDA product code for REUSABLE LAPAROSCOPIC INSTRUMENTS is GCJ.

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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)K930666REUSABLE LAPAROSCOPIC INSTRUMENTS W/ ELECTROCAUTERYK924148DIAMOND-SHARP(R) TROCARSK924149ENDO I/A PROBEK920985SNOWDEN-PENCER IRRIGATION PUMPK920986SNOWDEN-PENCER HIGH FLOW INSUFFLATOR, SP/88-9700

View all 10 devices →

Related Devices (Code: GCJ)

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.

K262397CuratOR EX2742Eizo CorporationK260884UNIDRIVE Select SystemKarl Storz SE & CO. KGK260972OEV-271MUH LCD Monitor;OEV-321MUH LCD Monitor;OEV-431MUH LCD MonitorSony CorporationK261139VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)Freyja Healthcare, LLCK253541EZ-Close™ (EZ Close Port Site Closing Device, EZ Close MAX Port Site Closing Device, EZ Close II Port Site Closing Device)Medical ImpactK261614LED LCD Monitor (OEV-271H)Lg Electronics.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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