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FDA 510(k)

ENDO I/A PROBE

K-Number: K924149 · 1993-01-26

ApplicantSnowden-Pencer
Decision Date1993-01-26
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENDO I/A PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Snowden-Pencer. It received FDA 510(k) clearance on 1993-01-26 under 510(k) number K924149. 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 ENDO I/A PROBE?

ENDO I/A PROBE is a medical device that received FDA 510(k) clearance on 1993-01-26. The listed applicant is Snowden-Pencer. The 510(k) number is K924149.

When did ENDO I/A PROBE receive FDA 510(k) clearance?

ENDO I/A PROBE received FDA 510(k) clearance on 1993-01-26, under 510(k) number K924149.

Who is the listed applicant for ENDO I/A PROBE?

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 ENDO I/A PROBE?

The FDA product code for ENDO I/A PROBE 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/ ELECTROCAUTERYK930667REUSABLE LAPAROSCOPIC INSTRUMENTSK924148DIAMOND-SHARP(R) TROCARSK920985SNOWDEN-PENCER IRRIGATION PUMPK920986SNOWDEN-PENCER HIGH FLOW INSUFFLATOR, SP/88-9700

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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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