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FDA 510(k)

PINLOCK CONTAINER

K-Number: K770071 · 1977-02-24

ApplicantPerkins Mfg. Co.
Decision Date1977-02-24
Product CodeKDT
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

PINLOCK CONTAINER is the device name listed in this FDA 510(k) record. The listed applicant is Perkins Mfg. Co.. It received FDA 510(k) clearance on 1977-02-24 under 510(k) number K770071. The device is classified under product code KDT. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PINLOCK CONTAINER?

PINLOCK CONTAINER is a medical device that received FDA 510(k) clearance on 1977-02-24. The listed applicant is Perkins Mfg. Co.. The 510(k) number is K770071.

When did PINLOCK CONTAINER receive FDA 510(k) clearance?

PINLOCK CONTAINER received FDA 510(k) clearance on 1977-02-24, under 510(k) number K770071.

Who is the listed applicant for PINLOCK CONTAINER?

The FDA 510(k) record lists Perkins Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PINLOCK CONTAINER?

The FDA product code for PINLOCK CONTAINER is KDT.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Perkins Mfg. Co. 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.

K972136TV MONITOR (P12/17)K954222VIDEO ENHANCEMENT UNITK926348SC1000 SCAN CONVERTERK920550DISPLAY PROCESSOR - MODEL IDP5100K915232GRUNDIG ELECTRONICS VARIOUS MODELSK910384VIDEO ANNOTATOR MODEL PK2310

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Related Devices (Code: KDT)

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.

K873593BIOSURE SPECIMEN COLLECTION CONTAINERBiosure, Inc.K862665NOVACYTE-UXsirius Medical, Inc.K834579BIOSPAL 2400SHospal Medical Corp.K834412PRESERV PVA FIXATIVE 15ML-FORMALIN PKPreventive Diagnostics Corp.K833660PRESERV PVA FIXATIVE -MALIN PACKPreventive Diagnostics Corp.K823773PROVIAL II #006-010-0201Dynatech Corp.

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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