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FDA 510(k)

PINK CASSETTE CADDIE

K-Number: K893728 · 1989-09-18

Decision Date1989-09-18
Product CodeIXA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PINK CASSETTE CADDIE is the device name listed in this FDA 510(k) record. The listed applicant is Medical Technique Instruments, Inc.. It received FDA 510(k) clearance on 1989-09-18 under 510(k) number K893728. The device is classified under product code IXA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PINK CASSETTE CADDIE?

PINK CASSETTE CADDIE is a medical device that received FDA 510(k) clearance on 1989-09-18. The listed applicant is Medical Technique Instruments, Inc.. The 510(k) number is K893728.

When did PINK CASSETTE CADDIE receive FDA 510(k) clearance?

PINK CASSETTE CADDIE received FDA 510(k) clearance on 1989-09-18, under 510(k) number K893728.

Who is the listed applicant for PINK CASSETTE CADDIE?

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

What is the FDA product code for PINK CASSETTE CADDIE?

The FDA product code for PINK CASSETTE CADDIE is IXA.

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 Medical Technique Instruments, 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.

Related Devices (Code: IXA)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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