Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MODEL MCC - MKIV MICRO COMPUTER CONTROLS

K-Number: K940972 · 1994-06-02

Decision Date1994-06-02
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MODEL MCC - MKIV MICRO COMPUTER CONTROLS is the device name listed in this FDA 510(k) record. The listed applicant is Invacare Corp.. It received FDA 510(k) clearance on 1994-06-02 under 510(k) number K940972. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL MCC - MKIV MICRO COMPUTER CONTROLS?

MODEL MCC - MKIV MICRO COMPUTER CONTROLS is a medical device that received FDA 510(k) clearance on 1994-06-02. The listed applicant is Invacare Corp.. The 510(k) number is K940972.

When did MODEL MCC - MKIV MICRO COMPUTER CONTROLS receive FDA 510(k) clearance?

MODEL MCC - MKIV MICRO COMPUTER CONTROLS received FDA 510(k) clearance on 1994-06-02, under 510(k) number K940972.

Who is the listed applicant for MODEL MCC - MKIV MICRO COMPUTER CONTROLS?

The FDA 510(k) record lists Invacare Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL MCC - MKIV MICRO COMPUTER CONTROLS?

The FDA product code for MODEL MCC - MKIV MICRO COMPUTER CONTROLS is ITI.

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.

Other records listing Invacare Corp. 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.

View all 111 devices →

Related Devices (Code: ITI)

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.

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.

↑