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FDA 510(k)

WEYLAND EXTENSION VIBRATOR

K-Number: K822413 · 1983-06-08

ApplicantMedical Management Service, Inc.
Decision Date1983-06-08
Product CodeJFB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

WEYLAND EXTENSION VIBRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Medical Management Service, Inc.. It received FDA 510(k) clearance on 1983-06-08 under 510(k) number K822413. The device is classified under product code JFB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WEYLAND EXTENSION VIBRATOR?

WEYLAND EXTENSION VIBRATOR is a medical device that received FDA 510(k) clearance on 1983-06-08. The listed applicant is Medical Management Service, Inc.. The 510(k) number is K822413.

When did WEYLAND EXTENSION VIBRATOR receive FDA 510(k) clearance?

WEYLAND EXTENSION VIBRATOR received FDA 510(k) clearance on 1983-06-08, under 510(k) number K822413.

Who is the listed applicant for WEYLAND EXTENSION VIBRATOR?

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

What is the FDA product code for WEYLAND EXTENSION VIBRATOR?

The FDA product code for WEYLAND EXTENSION VIBRATOR is JFB.

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Related Devices (Code: JFB)

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

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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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