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FDA 510(k)

DUKKI

K-Number: K913544 · 1991-08-29

ApplicantPin Dot Products, Inc.
Decision Date1991-08-29
Product CodeINM
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

DUKKI is the device name listed in this FDA 510(k) record. The listed applicant is Pin Dot Products, Inc.. It received FDA 510(k) clearance on 1991-08-29 under 510(k) number K913544. The device is classified under product code INM. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUKKI?

DUKKI is a medical device that received FDA 510(k) clearance on 1991-08-29. The listed applicant is Pin Dot Products, Inc.. The 510(k) number is K913544.

When did DUKKI receive FDA 510(k) clearance?

DUKKI received FDA 510(k) clearance on 1991-08-29, under 510(k) number K913544.

Who is the listed applicant for DUKKI?

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

What is the FDA product code for DUKKI?

The FDA product code for DUKKI is INM.

Related Clinical Trials

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.

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Other records listing Pin Dot Products, 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.

K925258DYNAMIC PRESSURE MONITOR 2000M AND 2000CK913510MECHANICAL SHAPE SENSORK913509IMPALA WHEELSK913553PIN DOT GROWTH/DIAL LINKSK913548PIN DOT ALUMINUM PANK913511IMPALA AXLES

View all 14 devices →

Related Devices (Code: INM)

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.

K063521NISSIN PEDIATRIC SERIES WHEELCHAIRNissin Medical, Inc.K941738STRYKER 5050 STRECHAIRStryker MedicalK941569CAREMOR CLINERWinco, Inc.K933000RECLINING GERI CHAIRS W/CASTERS & LAP TRAYWinco, Inc.K926028BENCHESTheradapt Products, Inc.K926053ELD-ARONDAK CHAIRAlert Care, 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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