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FDA 510(k)

PATELLAR FAT PAD RETRACTOR

K-Number: K831248 · 1983-06-24

Decision Date1983-06-24
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PATELLAR FAT PAD RETRACTOR is the device name listed in this FDA 510(k) record. The listed applicant is Techmedica, Inc.. It received FDA 510(k) clearance on 1983-06-24 under 510(k) number K831248. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PATELLAR FAT PAD RETRACTOR?

PATELLAR FAT PAD RETRACTOR is a medical device that received FDA 510(k) clearance on 1983-06-24. The listed applicant is Techmedica, Inc.. The 510(k) number is K831248.

When did PATELLAR FAT PAD RETRACTOR receive FDA 510(k) clearance?

PATELLAR FAT PAD RETRACTOR received FDA 510(k) clearance on 1983-06-24, under 510(k) number K831248.

Who is the listed applicant for PATELLAR FAT PAD RETRACTOR?

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

What is the FDA product code for PATELLAR FAT PAD RETRACTOR?

The FDA product code for PATELLAR FAT PAD RETRACTOR is HRX.

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 Techmedica, 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 31 devices →

Related Devices (Code: HRX)

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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