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FDA 510(k)

PEANUT WAND, MODIFICATION

K-Number: K944067 · 1994-12-08

ApplicantIdeal Medical, Inc.
Decision Date1994-12-08
Product CodeGCS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PEANUT WAND, MODIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Ideal Medical, Inc.. It received FDA 510(k) clearance on 1994-12-08 under 510(k) number K944067. The device is classified under product code GCS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEANUT WAND, MODIFICATION?

PEANUT WAND, MODIFICATION is a medical device that received FDA 510(k) clearance on 1994-12-08. The listed applicant is Ideal Medical, Inc.. The 510(k) number is K944067.

When did PEANUT WAND, MODIFICATION receive FDA 510(k) clearance?

PEANUT WAND, MODIFICATION received FDA 510(k) clearance on 1994-12-08, under 510(k) number K944067.

Who is the listed applicant for PEANUT WAND, MODIFICATION?

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

What is the FDA product code for PEANUT WAND, MODIFICATION?

The FDA product code for PEANUT WAND, MODIFICATION is GCS.

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Other records listing Ideal Medical, 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.

K931115HATCHER STONE-EMBOLIS EXTRACTORK926335IDEAS PEANUT WANDK922161GRICE SOFT TISSUE BIOPSY KITK921922GRICE LAPAROSCOPIC SUTURING NEEDLEK915175REDDICK RETRACTORK914880DUAL BALLOON EMBOLECTOMY CATHETER

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Related Devices (Code: GCS)

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.

K944062LAPRASCOPIC GRASPERInstrument Makar, Inc.K933201AESCULAP TROCAR INSTRUMENT SETAesculap, Inc.K93276210.0MM SUCTION/IRRIGATION PROBE & TUBING KITInman Medical Corp.K933371IMC ENDOSCOPIC INSTRUMENT HOLDERInman Medical Corp.K924134LEISEGANG LAPAROSCOPIC IRRIGATION SYSTEM/ACCESSLeisegang Medical, Inc.K931340GRASP FORCEPS/SCISSORS/NEEDLE HOLDER/DISSECTORBaxter Healthcare 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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