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FDA 510(k)

MULTI-FLEX TABLE -- MODEL 101

K-Number: K870710 · 1987-06-09

Decision Date1987-06-09
Product CodeJFB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MULTI-FLEX TABLE -- MODEL 101 is the device name listed in this FDA 510(k) record. The listed applicant is Slenderizers Equipment Mfg., Inc.. It received FDA 510(k) clearance on 1987-06-09 under 510(k) number K870710. 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 MULTI-FLEX TABLE -- MODEL 101?

MULTI-FLEX TABLE -- MODEL 101 is a medical device that received FDA 510(k) clearance on 1987-06-09. The listed applicant is Slenderizers Equipment Mfg., Inc.. The 510(k) number is K870710.

When did MULTI-FLEX TABLE -- MODEL 101 receive FDA 510(k) clearance?

MULTI-FLEX TABLE -- MODEL 101 received FDA 510(k) clearance on 1987-06-09, under 510(k) number K870710.

Who is the listed applicant for MULTI-FLEX TABLE -- MODEL 101?

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

What is the FDA product code for MULTI-FLEX TABLE -- MODEL 101?

The FDA product code for MULTI-FLEX TABLE -- MODEL 101 is JFB.

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 Slenderizers Equipment Mfg., 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.

View all 7 devices →

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.

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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