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FDA 510(k)

15 MILLIMETER MALE AND FEMALE ADAPTERS

K-Number: K884072 · 1988-10-07

ApplicantEastmed Enterprises, Inc.
Decision Date1988-10-07
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

15 MILLIMETER MALE AND FEMALE ADAPTERS is the device name listed in this FDA 510(k) record. The listed applicant is Eastmed Enterprises, Inc.. It received FDA 510(k) clearance on 1988-10-07 under 510(k) number K884072. The device is classified under product code CAI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 15 MILLIMETER MALE AND FEMALE ADAPTERS?

15 MILLIMETER MALE AND FEMALE ADAPTERS is a medical device that received FDA 510(k) clearance on 1988-10-07. The listed applicant is Eastmed Enterprises, Inc.. The 510(k) number is K884072.

When did 15 MILLIMETER MALE AND FEMALE ADAPTERS receive FDA 510(k) clearance?

15 MILLIMETER MALE AND FEMALE ADAPTERS received FDA 510(k) clearance on 1988-10-07, under 510(k) number K884072.

Who is the listed applicant for 15 MILLIMETER MALE AND FEMALE ADAPTERS?

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

What is the FDA product code for 15 MILLIMETER MALE AND FEMALE ADAPTERS?

The FDA product code for 15 MILLIMETER MALE AND FEMALE ADAPTERS is CAI.

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Other records listing Eastmed Enterprises, Inc. as applicant

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Related Devices (Code: CAI)

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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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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