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FDA 510(k)

SHOULDER BOLSTER, KNEE, ANKLE & LEG SUPPORT PADS

K-Number: K882520 · 1988-07-18

ApplicantKarlin Technology, Inc.
Decision Date1988-07-18
Product CodeLWG
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SHOULDER BOLSTER, KNEE, ANKLE & LEG SUPPORT PADS is the device name listed in this FDA 510(k) record. The listed applicant is Karlin Technology, Inc.. It received FDA 510(k) clearance on 1988-07-18 under 510(k) number K882520. The device is classified under product code LWG. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHOULDER BOLSTER, KNEE, ANKLE & LEG SUPPORT PADS?

SHOULDER BOLSTER, KNEE, ANKLE & LEG SUPPORT PADS is a medical device that received FDA 510(k) clearance on 1988-07-18. The listed applicant is Karlin Technology, Inc.. The 510(k) number is K882520.

When did SHOULDER BOLSTER, KNEE, ANKLE & LEG SUPPORT PADS receive FDA 510(k) clearance?

SHOULDER BOLSTER, KNEE, ANKLE & LEG SUPPORT PADS received FDA 510(k) clearance on 1988-07-18, under 510(k) number K882520.

Who is the listed applicant for SHOULDER BOLSTER, KNEE, ANKLE & LEG SUPPORT PADS?

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

What is the FDA product code for SHOULDER BOLSTER, KNEE, ANKLE & LEG SUPPORT PADS?

The FDA product code for SHOULDER BOLSTER, KNEE, ANKLE & LEG SUPPORT PADS is LWG.

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Related Devices (Code: LWG)

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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