510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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Perspectum Ltd.

Oxford Oxfordshire, GB

PERSPECTUM LTD. appears in FDA device records in Oxford Oxfordshire, GB. FDA records list 8 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.

FDA records held for this company

510(k) clearances
8
PMA records
0
Recall records
0
Registered establishments
1

510(k) clearance history

FDA records hold 8 510(k) clearances for Perspectum Ltd. between 2020 and 2026. The busiest year on record is 2022, with 2. The most recent is 2026, with 1.

Clearances by year, as a table
510(k) clearance decisions for Perspectum Ltd., by decision year
YearClearances
20201
20211
20222
20231
20242
20261
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K253413LiverMultiScan (v6.0)LNHSubstantially Equivalent
K241925VitruvianScan (v1.0)LNHSubstantially Equivalent
K233930MRCP+ version 2 (MRCP+ v2)LLZSubstantially Equivalent
K230294CoverScan (CoverScan v1.1)LLZSubstantially Equivalent
K213960LiverMultiScan v5 (LMSv5)LNHSubstantially Equivalent
K212565CoverScan v1LLZSubstantially Equivalent
K203280Hepatica v1 (Hepatica v1.0.0)LNHSubstantially Equivalent
K202170LiverMultiScanLNHSubstantially Equivalent

Registered establishments

FDA registered establishments for Perspectum Ltd., with the product codes listed at each
RegistrationFEIEstablishmentAddressRegistration expiresProduct codes listed
30142325553014232555PERSPECTUM LTD.Gemini One, Oxford Oxfordshire OX4 2LL GB2026

Registration numbers link to the FDA registration and listing record for that establishment.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.

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Data as of , FDA export datePage updated Source: openFDA, public domain