Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

BK-6453 RIMMED ACRYLIC LAP TRAY KIT

K-Number: K813627 · 1982-01-19

Decision Date1982-01-19
Product CodeKNO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BK-6453 RIMMED ACRYLIC LAP TRAY KIT is the device name listed in this FDA 510(k) record. The listed applicant is Fred Sammons, Inc.. It received FDA 510(k) clearance on 1982-01-19 under 510(k) number K813627. The device is classified under product code KNO. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BK-6453 RIMMED ACRYLIC LAP TRAY KIT?

BK-6453 RIMMED ACRYLIC LAP TRAY KIT is a medical device that received FDA 510(k) clearance on 1982-01-19. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K813627.

When did BK-6453 RIMMED ACRYLIC LAP TRAY KIT receive FDA 510(k) clearance?

BK-6453 RIMMED ACRYLIC LAP TRAY KIT received FDA 510(k) clearance on 1982-01-19, under 510(k) number K813627.

Who is the listed applicant for BK-6453 RIMMED ACRYLIC LAP TRAY KIT?

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

What is the FDA product code for BK-6453 RIMMED ACRYLIC LAP TRAY KIT?

The FDA product code for BK-6453 RIMMED ACRYLIC LAP TRAY KIT is KNO.

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 Fred Sammons, 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 278 devices →

Related Devices (Code: KNO)

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.

↑