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FDA 510(k)

REDDICK RETRACTOR

K-Number: K915175 · 1992-04-29

ApplicantIdeal Medical, Inc.
Decision Date1992-04-29
Product CodeGAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

REDDICK RETRACTOR 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 1992-04-29 under 510(k) number K915175. The device is classified under product code GAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REDDICK RETRACTOR?

REDDICK RETRACTOR is a medical device that received FDA 510(k) clearance on 1992-04-29. The listed applicant is Ideal Medical, Inc.. The 510(k) number is K915175.

When did REDDICK RETRACTOR receive FDA 510(k) clearance?

REDDICK RETRACTOR received FDA 510(k) clearance on 1992-04-29, under 510(k) number K915175.

Who is the listed applicant for REDDICK RETRACTOR?

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 REDDICK RETRACTOR?

The FDA product code for REDDICK RETRACTOR is GAD.

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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.

K944067PEANUT WAND, MODIFICATIONK931115HATCHER STONE-EMBOLIS EXTRACTORK926335IDEAS PEANUT WANDK922161GRICE SOFT TISSUE BIOPSY KITK921922GRICE LAPAROSCOPIC SUTURING NEEDLEK914880DUAL BALLOON EMBOLECTOMY CATHETER

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Related Devices (Code: GAD)

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.

K152538JRP Wound SpreaderJ.R. Parker, LLCK151104OTELO LLSpineartK132645THORATRAK MICS RETRACTOR SYSTEM, RACK, BLADESMedtronic, Inc.K071775DASHEzsurgicalK050256APPLE MEDICAL/OB MOBIUS ELASTIC RETRACTORApple Medical Corp.K043602QUADRANT RETRACTOR SYSTEMMedtronic Sofamor Danek

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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